Canonical Allele Identifier: PA2825779255
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 859074
ClinVar RCV Id: RCV001065099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Asp1131Glu
CA394707962
NM_001134407.3:c.3393T>G
CA394707963
NM_001134407.3:c.3393T>A