Allele Registry

Canonical Allele Identifier: PA645374235

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000497759

ClinVar Variation:

432191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Ile695Ser	CA383999493 NM_000834.3:c.2084T>G