Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139541127A>GCA255331F9c.329A>G (p.Asp110Gly)
c.277+3741A>G (n.277+3741A>G)
n.282A>G
 ClinVar dbSNP
Xg.139541127A>TCA414437538F9c.329A>T (p.Asp110Val)
c.277+3741A>T (n.277+3741A>T)
n.282A>T
 dbSNP

Number of alleles fetched