All transcripts active for the SLC26A4 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     
00019237 7 solute carrier family 26, member 4 NM_000441.1 NP_000432.1 940
How to query  


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