G80A (p.Gly80Ala) variant of HCN1 (O60741)
G80A (p.Gly80Ala) in HCN1 (O60741) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
G80A (p.Gly80Ala) variant details
- p.Gly80Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available