Y261F (p.Tyr261Phe) variant of GRIN1 (Q05586)
Y261F (p.Tyr261Phe) in GRIN1 (Q05586) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
Y261F (p.Tyr261Phe) variant details
- p.Tyr261Phe
- rs893141433
- Uncertain significance
- Missense
- EBI: ['uncertain-significance']
- UniProt: Uncertain significance
- Structural context available