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