Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003633208 | SCV004475593 | likely benign | HNSHA due to aldolase A deficiency | 2023-02-23 | criteria provided, single submitter | clinical testing |