S19W (p.Ser19Trp) variant of STK11 (Q15831)
S19W (p.Ser19Trp) in STK11 (Q15831) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
S19W (p.Ser19Trp) variant details
- p.Ser19Trp
- gnomAD rs1426026332
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available