Allele Registry

Canonical Allele Identifier: PA331390

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.9275953622

ClinVar RCV:

RCV000428720

RCV000663086

RCV000707667

RCV001526105

ClinVar Variation:

90797

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His610Asn	CA019403 NM_000251.3:c.1828C>A