Allele Registry

Canonical Allele Identifier: PA315049

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000187697

RCV000495871

RCV001172368

RCV001265244

ClinVar Variation:

205710

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Val620Met	CA315048 NM_000834.3:c.1858G>A