Allele Registry

Canonical Allele Identifier: PA354744

Gene: GRIN2B HGNC NCBI

ClinVar RCV:

RCV000203067

RCV001172328

ClinVar Variation:

218471

HGVS (amino-acid)	Matching Registered Transcripts
NP_000825.2:p.Ser810Arg	CA249270 NM_000834.3:c.2430C>A CA383996507 NM_000834.3:c.2430C>G CA383996522 NM_000834.3:c.2428A>C