Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139561992C>ACA255413F9c.1307C>A (p.Ala436Glu)
n.1723+251C>A
c.1193C>A (p.Ala398Glu)
c.1178C>A (p.Ala393Glu)
ClinVar dbSNP
Xg.139561992C>TCA255416F9c.1307C>T (p.Ala436Val)
n.1723+251C>T
c.1193C>T (p.Ala398Val)
c.1178C>T (p.Ala393Val)
ClinVar dbSNP

Number of alleles fetched