Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58077255G>ACA343270FLNBc.502G>A (p.Gly168Ser)
n.645G>A
n.661G>A
n.647G>A
 ClinVar dbSNP
3g.58077255G>TCA353333575FLNBc.502G>T (p.Gly168Cys)
n.645G>T
n.661G>T
n.647G>T
 ClinVar dbSNP

Number of alleles fetched