Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.44388366C>ACA118868FGF10c.317G>T (p.Cys106Phe)
 ClinVar dbSNP
5g.44388366C=CA1543090626FGF10c.317G= (p.Cys106=)
 dbSNP

Number of alleles fetched