Folklore Clinical Variant Interpretation MCP

Version 1.7.0

Folklore MCP classifies and assesses germline variants under ACMG/AMP. It returns canonical identity, automated classification, reported criteria, annotation, source evidence and provenance. Gene profiles, ClinGen gene-disease assertions and linked biomedical literature complete the scientific workflow.

Classify a variant

Connect your MCP client to:

https://api.helena.bio/folklore/v1/mcp

Access is anonymous. Call classify_germline_variant:

{"name":"classify_germline_variant","arguments":{"assembly":"GRCh38","query":"NM_007294.4:c.68_69del"}}

Input: one public GRCh38 nuclear germline SNV or simple indel smaller than 50 bp. Accepted notation includes supported HGVS, SPDI, rsID and genomic coordinates. Preserve transcript versions and reference alleles.

A resolved identity with successful interpretation includes automated ACMG/AMP classification, reported criteria, annotations, source evidence and provenance. Submitted ClinVar assertions retain their own source attribution alongside the Folklore classification. A VUS is a classification outcome.