Varaico: Literature-Extracted Genetic Variants

Gene:STUB1
Variant:p.S23I
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STUB1

NM_005861.4:p.S23I

Associated Papers

Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.

Barraud S et al.

Neuroendocrinology, 2021

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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."