Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.149483005T>ACA356677IDSc.1394A>T (p.Gln465Leu)
c.761A>T (p.Gln254Leu)
c.1124A>T (p.Gln375Leu)
 ClinVar dbSNP
Xg.149483005T=CA2465004011IDSc.1394A= (p.Gln465=)
c.761A= (p.Gln254=)
c.1124A= (p.Gln375=)
 dbSNP

Number of alleles fetched