Varaico: Literature-Extracted Genetic Variants

Gene:FGF3
Variant:p.S156C
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FGF3

NM_005247.4:p.S156C

Associated Papers

Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population.

Vallian Broojeni J et al.

Plos One, 2023

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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."