Allele Registry

Canonical Allele Identifier: PA170089

Gene: GRIN2B HGNC NCBI

ClinVar Allele:

152907

ClinVar RCV:

RCV000132723

ClinVar Variation:

143189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Glu413Gly	CA170088 NM_000834.3:c.1238A>G