Allele Registry

Canonical Allele Identifier: PA2826731984

Gene: GRID2 HGNC NCBI

ClinVar Allele:

418553

ClinVar RCV:

RCV000490816

ClinVar Variation:

427806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273767.1:p.Arg615Trp	CA3012457 NM_001286838.1:c.1843C>T