Canonical Allele Identifier: PA2826628697
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428285
ClinVar RCV Id: RCV000491433 RCV003449281 RCV004003451 RCV002523978
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1079Pro
CA346760597
NM_001281492.2:c.3236T>C