Q19H (p.Gln19His) variant of CYP11B1 (P15538)
Q19H (p.Gln19His) in CYP11B1 (P15538) is a missense change. The record also includes structural context.
Q19H (p.Gln19His) variant details
- p.Gln19His
- ExAC rs753228911
- TOPMed rs753228911
- gnomAD rs753228911
- Missense
- Structural context available