Allele Registry

Canonical Allele Identifier: PA354197

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000209917

RCV000794240

ClinVar Variation:

224086

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Thr685Pro	CA354196 NM_000834.3:c.2053A>C