Canonical Allele Identifier: PA1139686379
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 961366
ClinVar RCV Id: RCV001235046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001127880.1:p.Thr120Ala
CA394715186
NM_001134408.2:c.358A>G