This image was acquired from
wikimedia. It was marked as Public Domain or CC0 and is free to use. To verify, go to the source and check the information there.
Keywords from Image Description:
CFTRdel. The human genome mutation is characterized by the deletion of three base pairs in the CFTR nucleotide sequence causing the loss of the amino acid phenylalanine located at position Oak Ridge National Laboratory Human Genome Project website federal government source PDUSGov Genetic diseases and disorders Original upload log