Your search for "hccs" returned 694 TaqMan® SNP Genotyping Assays
holocytochrome c synthase
The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]
CCHL, HCCS, LSDMCA1, MCOPS7, MLS, RGD1563855
Please enter the information below and press OK to send your cart to Core Services for purchase.