Canonical Allele Identifier: PA195582
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186694
ClinVar RCV Id: RCV000166329 RCV000232782 RCV001194027 RCV001594863 RCV003995501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys843Tyr
CA020680
NM_000251.3:c.2528G>A