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Alport Syndrome is a progressive renal disease with cochlear and ocular involvement. The most common form (∼80%) is inherited in an X‐linked pattern. X‐linked Alport Syndrome (XLAS) is caused by mutations in the type IV collagen alpha chain 5 (COL4A5). We have developed a curated disease‐specific database containing reported sequence variants in COL4A5. Currently the database archives a total of 520...