L11H (p.Leu11His) variant of GABRA1 (P14867)
L11H (p.Leu11His) in GABRA1 (P14867) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L11H (p.Leu11His) variant details
- p.Leu11His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available