Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.44660525C>ACA344333SPG11c.349G>T (p.Glu117Ter)
n.378G>T
n.294G>T
n.380G>T
n.364G>T
 ClinVar dbSNP
15g.44660525C=CA2173717594SPG11c.349G= (p.Glu117=)
n.378G=
n.294G=
n.380G=
n.364G=
 dbSNP

Number of alleles fetched