Canonical Allele Identifier: PA1139728107
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 932279
ClinVar RCV Id: RCV001200016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe410Ile
CA16020973
NM_001354304.2:c.1228T>A