Varaico: Literature-Extracted Genetic Variants

Gene:SPRY1
Variant:p.Q183P
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SPRY1

NM_001258038.2:p.Q183P

Associated Papers

Case report: Identification and clinical phenotypic analysis of novel mutation of the PPP1CB gene in NSLH2 syndrome.

He X et al.

Frontiers in Behavioral Neuroscience, 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."