P18Q (p.Pro18Gln) variant of FH (P07954)
P18Q (p.Pro18Gln) in FH (P07954) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
P18Q (p.Pro18Gln) variant details
- p.Pro18Gln
- 1000Genomes rs201887750
- ESP rs201887750
- ExAC rs201887750
- TOPMed rs201887750
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available