Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.79921662C>GCA170078ELOVL4c.504G>C (p.Leu168Phe)
 ClinVar dbSNP
6g.79921662C>TCA142271129ELOVL4c.504G>A (p.Leu168=)
 dbSNP gnomAD v4

Number of alleles fetched