G66S (p.Gly66Ser) variant of HCN1 (O60741)
G66S (p.Gly66Ser) in HCN1 (O60741) is a missense change. The record also includes structural context.
G66S (p.Gly66Ser) variant details
- p.Gly66Ser
- TOPMed rs1356150414
- gnomAD rs1356150414
- Missense
- Structural context available