S102F (p.Ser102Phe) variant of SLC2A2 (P11168)
S102F (p.Ser102Phe) in SLC2A2 (P11168) is a missense change. The record also includes structural context.
S102F (p.Ser102Phe) variant details
- p.Ser102Phe
- TOPMed rs1716037183
- Missense
- Structural context available