Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA658827399

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 560788

ClinVar RCV Id: RCV000679302 RCV001014370 RCV001226997 RCV003459650

ClinVar Variation Id: 1942809

ClinVar RCV Id: RCV002646987 RCV004066765

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val695Leu	CA033555 NM_000251.3:c.2083G>C CA346729206 NM_000251.3:c.2083G>T