Canonical Allele Identifier: PA2825138024
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1754238
ClinVar RCV Id: RCV003098292 RCV002364449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe219Tyr
CA386296623
NM_000277.3:c.656T>A