Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904839G>TCA414908483F8c.5558C>A (p.Ala1853Asp)
c.5453C>A (p.Ala1818Asp)
 dbSNP
Xg.154904839G>ACA255174F8c.5558C>T (p.Ala1853Val)
c.5453C>T (p.Ala1818Val)
 ClinVar dbSNP

Number of alleles fetched