Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58078777C>TCA341860FLNBc.602C>T (p.Ala201Val)
n.745C>T
n.761C>T
c.95C>T (p.Ala32Val)
n.747C>T
 ClinVar dbSNP
3g.58078777C=CA1367486679FLNBc.602C= (p.Ala201=)
n.745C=
n.761C=
c.95C= (p.Ala32=)
n.747C=
 dbSNP

Number of alleles fetched