Canonical Allele Identifier: PA2825778280
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1376829
ClinVar RCV Id: RCV001888187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127879.1:p.Ile116Ser
CA394715209
NM_001134407.3:c.347T>G