E776D (p.Glu776Asp) variant of GRIA2 (Glutamate receptor 2)
E776D (p.Glu776Asp) in GRIA2 (Glutamate receptor 2) is a missense change. The record also includes published literature.
E776D (p.Glu776Asp) variant details
- p.Glu776Asp
- Missense
- Cited in: AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. (PMID 31300657)