Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904975G>ACA255166F8c.5422C>T (p.Leu1808Phe)
c.5317C>T (p.Leu1773Phe)
 ClinVar dbSNP
Xg.154904975G=CA2466828470F8c.5422C= (p.Leu1808=)
c.5317C= (p.Leu1773=)
 dbSNP

Number of alleles fetched