Canonical Allele Identifier: PA658680296
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg249Thr
CA346740105
NM_000179.3:c.746G>C