Canonical Allele Identifier: PA2826627157
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg642Trp
CA010016
NM_001281492.2:c.1924C>T