Allele Registry

Canonical Allele Identifier: PA111466

Gene: GRIN2B HGNC NCBI

ClinVar Allele:

48260

ClinVar RCV:

RCV000032865

RCV002466416

ClinVar Variation:

39661

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Pro553Leu	CA130440 NM_000834.3:c.1658C>T