Allele Registry

Canonical Allele Identifier: PA645471150

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.5394602121

ClinVar RCV:

RCV000230826

RCV000575441

RCV003998753

ClinVar Variation:

237361

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp41Tyr	CA10581991 NM_000251.3:c.121G>T