Canonical Allele Identifier: PA1139727988
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 991616
ClinVar RCV Id: RCV001279859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile374Val
CA6748742
NM_001354304.2:c.1120A>G