Allele Registry

Canonical Allele Identifier: PA2826464659

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000479480

RCV000551068

RCV000581059

RCV000766532

RCV003470543

RCV004002307

ClinVar Variation:

419601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val523Ile	CA16617588 NM_001258281.1:c.1567G>A