Canonical Allele Identifier: PA891846910
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 575571
ClinVar RCV Id: RCV000697827
ClinVar Variation Id: 1754518
ClinVar RCV Id: RCV002364614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly221Arg
CA346731712
NM_000251.3:c.661G>A
CA346731713
NM_000251.3:c.661G>C