E50D (p.Glu50Asp) variant of CNGA1 (P29973)
E50D (p.Glu50Asp) in CNGA1 (P29973) is a missense change. The record also includes structural context.
E50D (p.Glu50Asp) variant details
- p.Glu50Asp
- TOPMed rs942474540
- Missense
- Structural context available
E50D (p.Glu50Asp) in CNGA1 (P29973) is a missense change. The record also includes structural context.