Canonical Allele Identifier: PA913192131
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 631116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys804Thr
CA346753976
NM_000179.3:c.2411A>C