Allele Registry

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Canonical Allele Identifier: PA658804096

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525694

ClinVar RCV Id: RCV000629895 RCV001015167 RCV004002779

ClinVar Variation Id: 821089

ClinVar RCV Id: RCV001015168 RCV004004541

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys773Asn	CA035333 NM_000251.3:c.2319G>C CA035357 NM_000251.3:c.2319G>T