Canonical Allele Identifier: PA2826625087
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly159Val
CA346740617
NM_001281492.2:c.476G>T