Canonical Allele Identifier: PA111388
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 88733
ClinVar RCV Id: RCV000074392
JSON-LD

Amino-acid Alleles

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