R19L (p.Arg19Leu) variant of ATP1A3 (P13637)
R19L (p.Arg19Leu) in ATP1A3 (P13637) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R19L (p.Arg19Leu) variant details
- p.Arg19Leu
- ExAC rs782596240
- TOPMed rs782596240
- gnomAD rs782596240
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available