V13I (p.Val13Ile) variant of CNGA1 (P29973)
V13I (p.Val13Ile) in CNGA1 (P29973) is a missense change. The record also includes structural context.
V13I (p.Val13Ile) variant details
- p.Val13Ile
- TOPMed rs1202147662
- Missense
- Structural context available
V13I (p.Val13Ile) in CNGA1 (P29973) is a missense change. The record also includes structural context.