Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center For Human Genetics And Laboratory Diagnostics, |
RCV001353239 | SCV001548382 | pathogenic | Autosomal dominant Alport syndrome | 2020-11-25 | criteria provided, single submitter | clinical testing |