Allele Registry

Canonical Allele Identifier: PA2826463362

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000167160

RCV000198455

RCV000587804

RCV000663108

RCV001248898

RCV003995565

RCV004535135

ClinVar Variation:

187433

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile208Val	CA022377 NM_001258281.1:c.622A>G