L47M (p.Leu47Met) variant of PDGFRA (P16234)
L47M (p.Leu47Met) in PDGFRA (P16234) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
L47M (p.Leu47Met) variant details
- p.Leu47Met
- gnomAD rs1265352306
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available