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.
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ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000186 11 Usher syndrome 1C (autosomal recessive, severe) NM_153676.3 NP_005700.2 593
How to query