Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.44305045G>CCA3258482FGF10n.577C>G (p.Arg193Gly)
c.577C>G (p.Arg193Gly)
dbSNP ExAC gnomAD
5g.44305045G>ACA118866FGF10n.577C>T (p.Arg193Ter)
c.577C>T (p.Arg193Ter)
ClinVar dbSNP

Number of alleles fetched