H13L (p.His13Leu) variant of TGFB2 (P61812)
H13L (p.His13Leu) in TGFB2 (P61812) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
H13L (p.His13Leu) variant details
- p.His13Leu
- gnomAD rs1656693157
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available