Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908822C>TCA127498APOEc.526C>T (p.Arg176Cys)
c.604C>T (p.Arg202Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908822C=CA2338167904APOEc.526C= (p.Arg176=)
c.604C= (p.Arg202=)
 ClinVar dbSNP

Number of alleles fetched