Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.116790097G>ACA6288931APOA5c.*31C>T (n.*31C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790097G>TCA2580600885APOA5c.*31C>A (n.*31C>A)
dbSNP
11g.116790097G=CA2002739797APOA5c.*31C= (n.*31C=)
dbSNP

Number of alleles fetched