Allele Registry

Canonical Allele Identifier: PA2826465891

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000526536

RCV001193289

RCV001987337

RCV002289718

RCV002431522

RCV004003750

ClinVar Variation:

455578

1436368

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Phe821Leu	CA346731428 NM_001258281.1:c.2461T>C CA346731439 NM_001258281.1:c.2463C>A CA346731442 NM_001258281.1:c.2463C>G