Allele Registry

Canonical Allele Identifier: PA111473

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000149503

RCV001172367

ClinVar Variation:

162085

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Val618Gly	CA174968 NM_000834.3:c.1853T>G