A25G (p.Ala25Gly) variant of HCN1 (O60741)
A25G (p.Ala25Gly) in HCN1 (O60741) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
A25G (p.Ala25Gly) variant details
- p.Ala25Gly
- TOPMed rs1469192494
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available