Allele Registry

Canonical Allele Identifier: PA111388

Gene: GRIN2A HGNC NCBI

ClinVar RCV:

RCV000074392

ClinVar Variation:

88733

HGVS (amino-acid)	Matching Registered Transcripts
NP_000824.1:p.Phe652Val	CA145319 NM_000833.5:c.1954T>G