Allele Registry

Canonical Allele Identifier: PA2826465924

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000470535

RCV000569475

RCV001560001

RCV001844163

RCV003470452

RCV004000795

ClinVar Variation:

408555

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu832Ala	CA16610851 NM_001258281.1:c.2495A>C