Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58077271C>TCA253856FLNBc.518C>T (p.Ala173Val)
n.661C>T
n.677C>T
n.663C>T
 ClinVar dbSNP
3g.58077271C=CA1367486073FLNBc.518C= (p.Ala173=)
n.661C=
n.677C=
n.663C=
 dbSNP

Number of alleles fetched