Canonical Allele Identifier: PA2826625175
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231328
ClinVar RCV Id: RCV000221676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser179Thr
CA10578054
NM_001281492.2:c.535T>A