Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.149482894C>GCA255270IDSc.1505G>C (p.Trp502Ser)
c.872G>C (p.Trp291Ser)
c.1235G>C (p.Trp412Ser)
 ClinVar dbSNP
Xg.149482894C>TCA414517946IDSc.1505G>A (p.Trp502Ter)
c.872G>A (p.Trp291Ter)
c.1235G>A (p.Trp412Ter)
 ClinVar dbSNP

Number of alleles fetched