Canonical Allele Identifier: PA2825087349
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1766268
ClinVar RCV Id: RCV002371322
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly308Cys
CA346740743
NM_000179.3:c.922G>T