Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102855229C>TCA229656PAHc.613G>A (p.Glu205Lys)
c.598G>A (p.Glu200Lys)
n.709G>A
 ClinVar dbSNP
12g.102855229C=CA2059449450PAHc.613G= (p.Glu205=)
c.598G= (p.Glu200=)
n.709G=
 dbSNP

Number of alleles fetched