Allele Registry

Canonical Allele Identifier: PA658671692

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.6716586618

ClinVar RCV:

RCV000527224

RCV000562713

RCV000781569

RCV001284653

ClinVar Variation:

455593

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val155Gly	CA346730532 NM_000251.3:c.464T>G