Allele Registry

Canonical Allele Identifier: PA645374142

Gene: GRIN2B HGNC NCBI

ClinVar Variation Id: 423644

ClinVar RCV Id: RCV000481414

ClinVar Variation Id: 2947096

ClinVar RCV Id: RCV003801286

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Phe12Leu	CA6461472 NM_000834.3:c.36C>G CA16619495 NM_000834.3:c.36C>A CA384055132 NM_000834.3:c.34T>C