Canonical Allele Identifier: PA2826625828
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro332Thr
CA10578068
NM_001281492.2:c.994C>A