Q91H (p.Gln91His) variant of SLC2A2 (P11168)
Q91H (p.Gln91His) in SLC2A2 (P11168) is a missense change. The record also includes structural context.
Q91H (p.Gln91His) variant details
- p.Gln91His
- TOPMed rs1163149975
- Missense
- Structural context available