Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139541076A>GCA255322F9c.278A>G (p.Asp93Gly)
c.277+3690A>G (n.277+3690A>G)
n.242-11A>G
 ClinVar dbSNP
Xg.139541076A>TCA414437358F9c.278A>T (p.Asp93Val)
c.277+3690A>T (n.277+3690A>T)
n.242-11A>T
 dbSNP

Number of alleles fetched