Canonical Allele Identifier: PA915963655
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser315Pro
CA346740783
NM_000179.3:c.943T>C