Canonical Allele Identifier: PA916037481
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 446524
ClinVar RCV Id: RCV000515792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg169Pro
CA386299458
NM_001354304.2:c.506G>C