Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Servicio de Hematología y Oncología médica, |
RCV001779970 | SCV002016208 | pathogenic | Hereditary antithrombin deficiency | no assertion criteria provided | research | AntiFXa 33%; Ag 45% |