Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44907853T>CCA041808APOEc.137T>C (p.Leu46Pro)
c.215T>C (p.Leu72Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44907853T>ACA406303362APOEc.137T>A (p.Leu46Gln)
c.215T>A (p.Leu72Gln)
 dbSNP

Number of alleles fetched