Allele Registry

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Canonical Allele Identifier: PA337982

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216354

ClinVar RCV Id: RCV000198539 RCV000569330 RCV002273983 RCV002288815 RCV003493487 RCV003462325 RCV003997020

ClinVar Variation Id: 1019094

ClinVar RCV Id: RCV001318479 RCV002447347

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln793His	CA035514 NM_000251.3:c.2379G>T CA346730096 NM_000251.3:c.2379G>C