Probe set 204976_s_at


Probe set features
Probe set ID: 204976_s_at
Species: Homo sapiens
Array: Human Genome U133 Plus 2.0 Array
Type: Consensus sequence
Corresponding gene: ENSG00000101935 (Ensembl)  Q9Y4X0 / AMMECR1 / Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
9949 (EntrezGene)  AMMECR1 / AMMERC1|MFHIEN / Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
 
Best blastX hit on Uniprot:




 

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