Allele Registry

Canonical Allele Identifier: PA645374254

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000214028

RCV001172330

RCV003489375

ClinVar Variation:

234546

2690619

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Met818Leu	CA10577444 NM_000834.3:c.2452A>C CA383996414 NM_000834.3:c.2452A>T