Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Diagnostics Laboratory, |
RCV001375866 | SCV001572794 | likely pathogenic | Congenital hyperammonemia, type I | 2021-02-24 | criteria provided, single submitter | clinical testing |