R19G (p.Arg19Gly) variant of KIT (P10721)
R19G (p.Arg19Gly) in KIT (P10721) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R19G (p.Arg19Gly) variant details
- p.Arg19Gly
- gnomAD rs1490714621
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available