G92R (p.Gly92Arg) variant of HCN1 (O60741)
G92R (p.Gly92Arg) in HCN1 (O60741) is a missense change. The record also includes structural context.
G92R (p.Gly92Arg) variant details
- p.Gly92Arg
- TOPMed rs1413239994
- gnomAD rs1413239994
- Missense
- Structural context available