Allele Registry

Canonical Allele Identifier: PA111457

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000149504

RCV001172364

ClinVar Variation:

162086

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Asn615Ile	CA174969 NM_000834.3:c.1844A>T