Allele Registry

Canonical Allele Identifier: PA658737574

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000582679

RCV001321827

RCV002282243

RCV002417453

RCV003459442

ClinVar Variation:

491743

1784516

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu358Asp	CA346733277 NM_000251.3:c.1074G>C CA346733278 NM_000251.3:c.1074G>T