Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.155022464T>ACA255047F8c.89A>T (p.Glu30Val)
c.38+4316A>T (n.38+4316A>T)
c.71A>T (p.Glu24Val)
 ClinVar dbSNP
Xg.155022464T>CCA414920550F8c.89A>G (p.Glu30Gly)
c.38+4316A>G (n.38+4316A>G)
c.71A>G (p.Glu24Gly)
 ClinVar dbSNP

Number of alleles fetched