Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908786A>GCA127506APOEc.490A>G (p.Lys164Glu)
c.568A>G (p.Lys190Glu)
 ClinVar dbSNP gnomAD v4
19g.44908786A>CCA127507APOEc.490A>C (p.Lys164Gln)
c.568A>C (p.Lys190Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched