Allele Registry

Canonical Allele Identifier: PA645507281

Gene: GRIN2D HGNC NCBI

ClinVar RCV:

RCV000257970

ClinVar Variation:

267211

HGVS (amino-acid)	Matching Registered Transcripts
NP_000827.2:p.Val667Ile	CA10590055 NM_000836.2:c.1999G>A