Canonical Allele Identifier: PA094868
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91109
ClinVar RCV Id: RCV000076612 RCV000491974 RCV001249918 RCV001293544 RCV001390798 RCV003452944
ClinVar Variation Id: 1744045
ClinVar RCV Id: RCV002340695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly164Arg
CA021212
NM_000251.3:c.490G>A
CA346730633
NM_000251.3:c.490G>C