Canonical Allele Identifier: PA2825087427
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1809567
ClinVar RCV Id: RCV002481146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg316Thr
CA346740803
NM_000179.3:c.947G>C