There are different genetic variant types such as Indels, SNPs, insertions/deletions etc.
In ClinVar database, these variants are given a long name. Examples - NM_172201.1(KCNE2):c.79C>T (p.Arg27Cys). But in other instances like in publications and clinical reports, this full name is not used to refer to that variant. Can I take the gene name (KCNE2) and genetic code change (c.79C>T) together? What are the other possible ways to refer to a variant? Can I take the position (p.Arg27Cys) as well? I want this to extract information about genetic variants from publications and clinical reports.