Canonical Allele Identifier: PA916037646
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102851
ClinVar RCV Id: RCV000089112 RCV000148723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Lys274Glu
CA229786
NM_001354304.2:c.820A>G