Canonical Allele Identifier: PA2573163687
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391982
ClinVar RCV Id: RCV001893362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met799Val
CA346753877
NM_000179.3:c.2395A>G