Canonical Allele Identifier: PA2826625090
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 928046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly159Arg
CA346740612
NM_001281492.2:c.475G>C