Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003056710 | SCV003446380 | likely benign | HNSHA due to aldolase A deficiency | 2023-06-22 | criteria provided, single submitter | clinical testing |