Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA2826464959

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783638

ClinVar RCV Id: RCV002423510

ClinVar Variation Id: 2447339

ClinVar RCV Id: RCV003176395

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Phe591Leu	CA346728823 NM_001258281.1:c.1771T>C CA346728829 NM_001258281.1:c.1773T>A CA346728831 NM_001258281.1:c.1773T>G