Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21006288C>TCA022750APOBc.10580G>A (p.Arg3527Gln)
c.5869+4445G>A (n.5869+4445G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006288C>ACA345986090APOBc.10580G>T (p.Arg3527Leu)
c.5869+4445G>T (n.5869+4445G>T)
 ClinVar dbSNP

Number of alleles fetched