Allele Registry

Canonical Allele Identifier: PA658672728

Gene: MSH2 HGNC NCBI

MaveDb:

Score -5.6656755878

ClinVar RCV:

RCV000556013

RCV000570637

RCV000588090

RCV003470712

ClinVar Variation:

455526

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val598Met	CA031369 NM_000251.3:c.1792G>A