Varaico: Literature-Extracted Genetic Variants

Gene:SCT
Variant:p.K56N
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SCT

NM_021920.4:p.K56N

Associated Papers

Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.

S UK et al.

Molecules (basel, Switzerland), 2020

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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."