Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139541126G>TCA414437535F9c.328G>T (p.Asp110Tyr)
c.277+3740G>T (n.277+3740G>T)
n.281G>T
 dbSNP
Xg.139541126G>ACA255435F9c.328G>A (p.Asp110Asn)
c.277+3740G>A (n.277+3740G>A)
n.281G>A
 ClinVar dbSNP COSMIC

Number of alleles fetched