Canonical Allele Identifier: PA2573206260
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1693239
ClinVar RCV Id: RCV002260498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu333Pro
CA16020917
NM_001354304.2:c.998T>C