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- databases for immunodeficiency-causing variations

   NCF1base
   Variation registry for  Autosomal recessive p47phox deficiency



Other resources

OMIM resources



NCF1 Reference Sequences
Sequence type Accession number Description
Genomic sequence IDRefSeq: D0099
 
DNA Sequences exons 1-5: EMBL: U57833
exons 6-8: EMBL: U57834
exons 9-11: EMBL: U57835
 
mRNA IDRefSeq: C0099
EMBL: M21186
 
Amino Acid Sequence P14598