Q49H (p.Gln49His) variant of LEP (Leptin)
Q49H (p.Gln49His) in LEP (Leptin) is a missense change. The record also includes structural context.
Q49H (p.Gln49His) variant details
- p.Gln49His
- TOPMed rs1795310969
- Missense
- Structural context available
Q49H (p.Gln49His) in LEP (Leptin) is a missense change. The record also includes structural context.