Canonical Allele Identifier: PA2825088688
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2084293
ClinVar RCV Id: RCV003011065 RCV004068428
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr589His
CA346749094
NM_000179.3:c.1765T>C