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Date: 2018-03-06 08:50:01 | Exercise A variant has been identified in a patient presenting with a genetic disorder. We’d like to determine if it is causing the phenotype. The variant is in HGVS notation: 21:g.25606478T>C. (a) What are the proteAdd to Reading ListSource URL: ftp.ebi.ac.ukDownload Document from Source WebsiteFile Size: 101,75 KBShare Document on Facebook |