Allele Registry

Canonical Allele Identifier: PA645376420

Gene: GRID2 HGNC NCBI

ClinVar Allele:

418553

ClinVar RCV:

RCV000490816

ClinVar Variation:

427806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001501.2:p.Arg710Trp	CA3012457 NM_001510.4:c.2128C>T