Allele Registry

Canonical Allele Identifier: PA130436

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000032862

ClinVar Variation:

39658

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Cys456Tyr	CA130435 NM_000834.3:c.1367G>A