Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908786A>CCA127507APOEc.490A>C (p.Lys164Gln)
c.568A>C (p.Lys190Gln)
ClinVar dbSNP gnomAD
19g.44908786A>GCA127506APOEc.490A>G (p.Lys164Glu)
c.568A>G (p.Lys190Glu)
ClinVar dbSNP

Number of alleles fetched