P17A (p.Pro17Ala) variant of HMGCR (P04035)
P17A (p.Pro17Ala) in HMGCR (P04035) is a missense change. The record also includes structural context.
P17A (p.Pro17Ala) variant details
- p.Pro17Ala
- gnomAD rs1416769598
- Missense
- Structural context available
P17A (p.Pro17Ala) in HMGCR (P04035) is a missense change. The record also includes structural context.