Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.44388443T>GCA118872FGF10c.240A>C (p.Arg80Ser)
ClinVar dbSNP
5g.44388443T>CCA444400475FGF10c.240A>G (p.Arg80=)
dbSNP gnomAD v4
5g.44388443T=CA1543090831FGF10c.240A= (p.Arg80=)
dbSNP

Number of alleles fetched