L28W (p.Leu28Trp) variant of FH (P07954)
L28W (p.Leu28Trp) in FH (P07954) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
L28W (p.Leu28Trp) variant details
- p.Leu28Trp
- rs2527345107
- ClinGen CA345442772
- ClinVar RCV003560341
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available