Canonical Allele Identifier: PA2826628267
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu953Lys
CA346758114
NM_001281492.2:c.2857G>A