Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.111410188C>TCA414246873DCXc.211G>A (p.Ala71Thr)
c.454G>A (p.Ala152Thr)
c.429G>A
n.451G>A
 ClinVar dbSNP
Xg.111410188C>ACA121609DCXc.211G>T (p.Ala71Ser)
c.454G>T (p.Ala152Ser)
c.429G>T
n.451G>T
 ClinVar dbSNP

Number of alleles fetched