Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154032206C>ACA233146MECP2c.413+1G>T (p.=)
c.98+1G>T (p.=)
c.377+1G>T (p.=)
c.-184+1G>T (p.=)
c.*431+1G>T (p.=)
n.2725+1G>T
c.365+1G>T (p.=)
ClinVar dbSNP
Xg.154032206C>TCA233145MECP2c.413+1G>A (p.=)
c.98+1G>A (p.=)
c.377+1G>A (p.=)
c.-184+1G>A (p.=)
c.*431+1G>A (p.=)
n.2725+1G>A
c.365+1G>A (p.=)
ClinVar dbSNP

Number of alleles fetched