Varaico: Literature-Extracted Genetic Variants

Gene:CFL2
Variant:p.C39G
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CFL2

NM_138638.5:p.C39G

Associated Papers

Novel missense variants in CFL2 affect F-actin depolymerisation and expand the disease spectrum of CFL2-related myopathy.

Dofash LNH et al.

Human Molecular Genetics, 2025

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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."