Canonical Allele Identifier: PA916037538
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102768
ClinVar RCV Id: RCV000089018 RCV000671113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu212Pro
CA229668
NM_001354304.2:c.635T>C