Allele Registry

Canonical Allele Identifier: PA645471654

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000491118

RCV000985813

RCV001053469

RCV001532970

RCV004003472

ClinVar Variation:

428533

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln170Arg	CA346730701 NM_000251.3:c.509A>G