Allele Registry

Canonical Allele Identifier: PA645475820

Gene: MSH2 HGNC NCBI

MaveDb:

Score 2.5414479068

ClinVar Allele:

419414

ClinVar RCV:

RCV000490997

RCV003449375

ClinVar Variation:

428545

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His801Pro	CA346730191 NM_000251.3:c.2402A>C