P17A (p.Pro17Ala) variant of MCCC2 (Q9HCC0)
P17A (p.Pro17Ala) in MCCC2 (Q9HCC0) is a missense change. The record also includes structural context.
P17A (p.Pro17Ala) variant details
- p.Pro17Ala
- ExAC rs780891559
- TOPMed rs780891559
- gnomAD rs780891559
- Missense
- Structural context available