F98L (p.Phe98Leu) variant of HCN1 (O60741)
F98L (p.Phe98Leu) in HCN1 (O60741) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F98L (p.Phe98Leu) variant details
- p.Phe98Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available