Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102852861T>CCA229765PAHc.796A>G (p.Thr266Ala)
c.781A>G (p.Thr261Ala)
n.555A>G
 ClinVar dbSNP
12g.102852861T>GCA267673PAHc.796A>C (p.Thr266Pro)
c.781A>C (p.Thr261Pro)
n.555A>C
 ClinVar dbSNP

Number of alleles fetched