Canonical Allele Identifier: PA916037347
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805803
ClinVar RCV Id: RCV000993598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser16Tyr
CA16020719
NM_001354304.2:c.47C>A