T47P (p.Thr47Pro) variant of CNGA1 (P29973)
T47P (p.Thr47Pro) in CNGA1 (P29973) is a missense change. The record also includes structural context.
T47P (p.Thr47Pro) variant details
- p.Thr47Pro
- TOPMed rs1304247434
- Missense
- Structural context available
T47P (p.Thr47Pro) in CNGA1 (P29973) is a missense change. The record also includes structural context.