A26T (p.Ala26Thr) variant of GRIN2A (Q12879)
A26T (p.Ala26Thr) in GRIN2A (Q12879) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
A26T (p.Ala26Thr) variant details
- p.Ala26Thr
- 1000Genomes rs751198815
- ExAC rs751198815
- TOPMed rs751198815
- gnomAD rs751198815
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available