Allele Registry

Canonical Allele Identifier: PA645474195

Gene: MSH2 HGNC NCBI

MaveDb:

Score -1.4627938846

ClinVar RCV:

RCV000231260

RCV001183558

ClinVar Variation:

237360

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys393Gln	CA10582009 NM_000251.3:c.1177A>C