Allele Registry

Canonical Allele Identifier: PA645476060

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.2258755089

ClinVar RCV:

RCV000221700

RCV000524618

ClinVar Variation:

233504

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu881Gln	CA10578013 NM_000251.3:c.2641G>C