Allele Registry

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Canonical Allele Identifier: PA169108

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90868

ClinVar RCV Id: RCV000076370 RCV000132039 RCV000202225 RCV000524373 RCV001264415 RCV001588897 RCV003452883

ClinVar Variation Id: 2673350

ClinVar RCV Id: RCV003455975

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly683Arg	CA019900 NM_000251.3:c.2047G>A CA346729142 NM_000251.3:c.2047G>C