Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.153740195T>CCA278375ABCD1c.1592T>C (p.Leu531Pro)
n.595T>C
n.2064T>C
 ClinVar dbSNP
Xg.153740195T=CA2466456444ABCD1c.1592T= (p.Leu531=)
n.595T=
n.2064T=
 dbSNP

Number of alleles fetched