P38A (p.Pro38Ala) variant of FH (P07954)
P38A (p.Pro38Ala) in FH (P07954) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P38A (p.Pro38Ala) variant details
- p.Pro38Ala
- Ensembl rs2147926866
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available