Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA2579909596

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775034

ClinVar RCV Id: RCV002403358

ClinVar Variation Id: 1775234

ClinVar RCV Id: RCV002405387 RCV004007332 RCV003759682

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu52Pro	CA029520 NM_000251.3:c.155T>C CA2580066882 NM_000251.3:c.155_156delinsCT