Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154956979G>ACA255120F8c.1730C>T (p.Ser577Phe)
c.*1606C>T (n.*1606C>T)
c.1625C>T (p.Ser542Phe)
 ClinVar dbSNP COSMIC COSMIC
Xg.154956979G=CA2466845308F8c.1730C= (p.Ser577=)
c.*1606C= (n.*1606C=)
c.1625C= (p.Ser542=)
 dbSNP

Number of alleles fetched