Canonical Allele Identifier: PA2826626438
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 953142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr477Ala
CA346749445
NM_001281492.2:c.1429A>G