Allele Registry

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Canonical Allele Identifier: PA645474758

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422757

ClinVar RCV Id: RCV000478694 RCV001219407 RCV002413333

ClinVar Variation Id: 919975

ClinVar RCV Id: RCV001178455 RCV001221393

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val611Leu	CA16617593 NM_000251.3:c.1831G>C CA346728374 NM_000251.3:c.1831G>T