Allele Registry

Canonical Allele Identifier: PA331497

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076445

RCV000508314

RCV000561670

RCV000680198

RCV001014940

RCV003452902

RCV003593976

ClinVar Variation:

90943

439192

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly751Arg	CA020361 NM_000251.3:c.2251G>A CA346729765 NM_000251.3:c.2251G>C