Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908804G>CCA042396APOEc.508G>C (p.Ala170Pro)
c.586G>C (p.Ala196Pro)
 ClinVar dbSNP
19g.44908804G=CA2338167893APOEc.508G= (p.Ala170=)
c.586G= (p.Ala196=)
 dbSNP

Number of alleles fetched