Allele Registry

Canonical Allele Identifier: PA111437

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000149505

RCV001260644

RCV002293420

RCV002514867

ClinVar Variation:

162087

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Arg540His	CA174970 NM_000834.3:c.1619G>A