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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 disease2024-06-25
1.0
ClinGen VHL Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for VHL Version 1.0.0VHL
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