L11A (p.Leu11Ala) variant of FGFR4 (P22455)
L11A (p.Leu11Ala) in FGFR4 (P22455) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
L11A (p.Leu11Ala) variant details
- p.Leu11Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available