Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58078804G>TCA341864FLNBc.629G>T (p.Gly210Val)
n.772G>T
n.788G>T
c.122G>T (p.Gly41Val)
n.774G>T
 ClinVar dbSNP
3g.58078804G=CA1367486687FLNBc.629G= (p.Gly210=)
n.772G=
n.788G=
c.122G= (p.Gly41=)
n.774G=
 dbSNP

Number of alleles fetched