Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Division of Genetics, |
RCV003234958 | SCV003934897 | likely pathogenic | Autosomal dominant centronuclear myopathy | 2023-06-15 | criteria provided, single submitter | research |