Canonical Allele Identifier: PA645379259
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys317Arg
CA10577261
NM_000179.3:c.950A>G