Allele Registry

Canonical Allele Identifier: PA095025

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000215108

RCV000524393

RCV000662762

RCV001030485

RCV001174808

RCV003997164

ClinVar Variation:

90995

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys845Glu	CA020689 NM_000251.3:c.2533A>G