Allele Registry

Canonical Allele Identifier: PA645471142

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000483915

RCV000579393

RCV000629871

ClinVar Variation:

422949

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg35Gly	CA16617549 NM_000251.3:c.103C>G