Allele Registry

Canonical Allele Identifier: PA658673193

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000526536

RCV001193289

RCV001987337

RCV002289718

RCV002431522

RCV004003750

ClinVar Variation:

455578

1436368

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Phe887Leu	CA346731428 NM_000251.3:c.2659T>C CA346731439 NM_000251.3:c.2661C>A CA346731442 NM_000251.3:c.2661C>G