{{Rsnum
|rsid=76212747
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PAH
|position=102852923
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=76212747
|variant=0059
}}{{ClinVar
|rsid=76212747
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=103246701
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000000000402110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.103246701A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612349.0059
|CLNSIG=5
|CLNCUI=C0751435
|CLNDBN=Hyperphenylalaninemia, non-pku
|Disease=Hyperphenylalaninemia
|CLNACC=RCV000000664.1
|Tags=RV;PM;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C0751435
}}