P77A (p.Pro77Ala) variant of NLGN3 (Neuroligin-3)
P77A (p.Pro77Ala) in NLGN3 (Neuroligin-3) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P77A (p.Pro77Ala) variant details
- p.Pro77Ala
- TOPMed rs1211820354
- gnomAD rs1211820354
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available