Canonical Allele Identifier: PA645379292
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410402
ClinVar RCV Id: RCV002230102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser328Thr
CA16610903
NM_000179.3:c.983G>C