Canonical Allele Identifier: PA913195052
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619163
ClinVar RCV Id: RCV000758127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe233Ile
CA16020843
NM_000277.3:c.697T>A