Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Genomic Medicine, |
RCV001420453 | SCV001622489 | likely pathogenic | Congenital prothrombin deficiency | 2021-04-28 | criteria provided, single submitter | research |