V138A (p.Val138Ala) variant of CDH2 (Cadherin-2)
V138A (p.Val138Ala) in CDH2 (Cadherin-2) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V138A (p.Val138Ala) variant details
- p.Val138Ala
- TOPMed rs1393606084
- gnomAD rs1393606084
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available