Allele Registry

Canonical Allele Identifier: PA315047

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV001172347

RCV001852459

ClinVar Variation:

205709

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Ile150Val	CA315046 NM_000834.3:c.448A>G