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Effortless mutation search and display tool
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Gene: PRPS1 & Disease: Rare X-Linked Non-Syndromic Sensorineural Deafness Type Dfn, 2 results
ClinVar | Gene | Nucleotide | Amino Acid | Transcript ID | Mutation type | Clinical Significance | Disease count | Publications |
|---|---|---|---|---|---|---|---|---|
-- | Dup | 5 + | 0 | |||||
-- | Dup | 5 + | 0 |
2 Results, 20 per Page
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