Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Servicio de Hematología y Oncología médica, |
RCV001779978 | SCV002016216 | pathogenic | Hereditary antithrombin deficiency | no assertion criteria provided | research | AntiFXa 54%; Ag 56% |