R92G (p.Arg92Gly) variant of LEP (Leptin)
R92G (p.Arg92Gly) in LEP (Leptin) is a missense change. The record also includes structural context.
R92G (p.Arg92Gly) variant details
- p.Arg92Gly
- ExAC rs745576625
- TOPMed rs745576625
- gnomAD rs745576625
- Missense
- Structural context available