Allele Registry

Canonical Allele Identifier: PA2826731909

Gene: GRID2 HGNC NCBI

ClinVar RCV:

RCV001777096

RCV003913375

ClinVar Variation:

1321117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273767.1:p.Thr68Met	CA3011900 NM_001286838.1:c.203C>T