Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154957049T>CCA255116F8c.1660A>G (p.Ser554Gly)
c.*1536A>G (n.*1536A>G)
c.1555A>G (p.Ser519Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154957049T=CA2466845339F8c.1660A= (p.Ser554=)
c.*1536A= (n.*1536A=)
c.1555A= (p.Ser519=)
 dbSNP

Number of alleles fetched