Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58077235T>GCA130016FLNBc.482T>G (p.Phe161Cys)
n.625T>G
n.641T>G
n.627T>G
 ClinVar dbSNP
3g.58077235T=CA1367486062FLNBc.482T= (p.Phe161=)
n.625T=
n.641T=
n.627T=
 dbSNP

Number of alleles fetched