Canonical Allele Identifier: PA645474275
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246389
ClinVar RCV Id: RCV000236876 RCV001061266 RCV003454720
ClinVar Variation Id: 818775
ClinVar RCV Id: RCV001010702 RCV003336230 RCV003594068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly426Arg
CA10584213
NM_000251.3:c.1276G>A
CA346734314
NM_000251.3:c.1276G>C