Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102855138T>GCA229700PAHc.704A>C (p.Gln235Pro)
c.689A>C (p.Gln230Pro)
n.800A>C
 ClinVar dbSNP
12g.102855138T=CA2059449022PAHc.704A= (p.Gln235=)
c.689A= (p.Gln230=)
n.800A=
 dbSNP

Number of alleles fetched