All transcripts active for the USH1C gene


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
1 entry on 1 page. Showing entry 1.
How to query  

ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000186 11 Usher syndrome 1C (autosomal recessive, severe) NM_153676.3 NP_005700.2 613
How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.