P56H (p.Pro56His) variant of CNGA1 (P29973)
P56H (p.Pro56His) in CNGA1 (P29973) is a missense change. The record also includes structural context.
P56H (p.Pro56His) variant details
- p.Pro56His
- cosmic curated COSV10065
- TOPMed rs1291858210
- gnomAD rs1291858210
- Missense
- Structural context available