P2A (p.Pro2Ala) variant of BMPR1A (P36894)
P2A (p.Pro2Ala) in BMPR1A (P36894) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
P2A (p.Pro2Ala) variant details
- p.Pro2Ala
- 1000Genomes rs11528010
- ESP rs11528010
- ExAC rs11528010
- TOPMed rs11528010
- Benign
- Missense
- EBI: Benign (in dbSNP:rs11528010)
- UniProt: Benign (in dbSNP:rs11528010)
- Structural context available