C26W (p.Cys26Trp) variant of ERBB2 (P04626)
C26W (p.Cys26Trp) in ERBB2 (P04626) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
C26W (p.Cys26Trp) variant details
- p.Cys26Trp
- TOPMed rs1021403569
- gnomAD rs1021403569
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available