L14V (p.Leu14Val) variant of ALK (ALK tyrosine kinase receptor)
L14V (p.Leu14Val) in ALK (ALK tyrosine kinase receptor) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
L14V (p.Leu14Val) variant details
- p.Leu14Val
- TOPMed rs1667971309
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available