Allele Registry

Canonical Allele Identifier: PA645471272

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.463943352

ClinVar RCV:

RCV000460763

RCV000523794

RCV000575381

RCV004000791

ClinVar Variation:

408535

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met83Val	CA16610775 NM_000251.3:c.247A>G