Canonical Allele Identifier: PA2826629237
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059451
ClinVar RCV Id: RCV001368735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1187Arg
CA346761521
NM_001281492.2:c.3560A>G