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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000551.4(VHL):c.408del (p.Phe136fs) | Pathogenic | von Hippel-Lindau disease | 2024-06-25 | 1.0 | ClinGen VHL Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for VHL Version 1.0.0 | VHL |
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