Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.58077270G>ACA269449FLNBc.517G>A (p.Ala173Thr)
n.660G>A
n.676G>A
n.662G>A
 ClinVar dbSNP
3g.58077270G=CA1367486072FLNBc.517G= (p.Ala173=)
n.660G=
n.676G=
n.662G=
 dbSNP

Number of alleles fetched