Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.59030427T>CCA214974ATP5F1Ec.35A>G (p.Tyr12Cys)
n.739A>G
n.480A>G
 ClinVar dbSNP
20g.59030427T=CA2372584977ATP5F1Ec.35A= (p.Tyr12=)
n.739A=
n.480A=
 dbSNP

Number of alleles fetched