V39G (p.Val39Gly) variant of ABCC1 (P33527)
V39G (p.Val39Gly) in ABCC1 (P33527) is a missense change. The record also includes structural context.
V39G (p.Val39Gly) variant details
- p.Val39Gly
- Ensembl rs2047608117
- Missense
- Structural context available