A27G (p.Ala27Gly) variant of GRIN2A (Q12879)
A27G (p.Ala27Gly) in GRIN2A (Q12879) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A27G (p.Ala27Gly) variant details
- p.Ala27Gly
- gnomAD rs367543129
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available