F66L (p.Phe66Leu) variant of FHL1 (Q13642)
F66L (p.Phe66Leu) in FHL1 (Q13642) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F66L (p.Phe66Leu) variant details
- p.Phe66Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available