Allele Registry

Canonical Allele Identifier: PA645475511

Gene: MSH2 HGNC NCBI

MaveDb:

Score -5.0951645541

ClinVar RCV:

RCV000236064

RCV000556812

RCV000564620

RCV003469187

RCV003998917

ClinVar Variation:

246264

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp742Asn	CA10584222 NM_000251.3:c.2224G>A