Varaico: Literature-Extracted Genetic Variants

Gene:CLRN1
Variant:p.V101fs
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CLRN1

NM_052995.2:p.V101fs

Associated Papers

Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort.

Smirnov VM et al.

Investigative Ophthalmology & Visual Science, 2022

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."