Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58077195T>GCA353333429FLNBc.442T>G (p.Trp148Gly)
n.585T>G
n.601T>G
n.587T>G
 dbSNP COSMIC
3g.58077195T>ACA341841FLNBc.442T>A (p.Trp148Arg)
n.585T>A
n.601T>A
n.587T>A
 ClinVar dbSNP

Number of alleles fetched