Canonical Allele Identifier: PA913193504
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 619524
ClinVar RCV Id: RCV000758594
ClinVar Variation Id: 863985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly827Arg
CA46707600
NM_000251.3:c.2479G>A
CA346730597
NM_000251.3:c.2479G>C