All transcripts active for the USH2A 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     
00000008 1 Usher syndrome 2A (autosomal recessive, mild), transcript variant 2 NM_206933.2 NP_996816.2 11589
How to query