E98D (p.Glu98Asp) variant of ABCC9 (O60706)
E98D (p.Glu98Asp) in ABCC9 (O60706) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E98D (p.Glu98Asp) variant details
- p.Glu98Asp
- gnomAD rs1466134448
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available