Allele Registry

Canonical Allele Identifier: PA111427

Gene: GRIN2A HGNC NCBI

ClinVar RCV:

RCV000074389

RCV001557828

ClinVar Variation:

88730

HGVS (amino-acid)	Matching Registered Transcripts
NP_000824.1:p.Thr531Met	CA145316 NM_000833.5:c.1592C>T