Allele Registry

Canonical Allele Identifier: PA197638

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000167160

RCV000198455

RCV000587804

RCV000663108

RCV001248898

RCV003995565

RCV004535135

ClinVar Variation:

187433

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile274Val	CA022377 NM_000251.3:c.820A>G