Canonical Allele Identifier: PA2826626416
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780462
ClinVar RCV Id: RCV002410055
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser472Thr
CA346749354
NM_001281492.2:c.1414T>A