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Variant Pathogenicity
TRDN
Name
TRDN
HGNC ID
HGNC:12261
Cytogenetic Location
6q22.31
Haploinsufficiency
Associated with Autosomal Recessive Phenotype
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ClinVar Variants
TRDN
-
catecholaminergic polymorphic ventricular tachycardia 5
| MONDO:0014191
Curated by
Classification
Date
Report
Gene Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
06/01/2017
View report
TRDN
Curated by
Classification
Date
Report
Gene Dosage Sensitivity
Gene Associated with Autosomal Recessive Phenotype
06/01/2017
View report
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