Canonical Allele Identifier: PA913193094
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 632900
ClinVar RCV Id: RCV000780445 RCV001869152 RCV002422667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala272Thr
CA346732768
NM_000251.3:c.814G>A