Canonical Allele Identifier: PA269922
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 133314
ClinVar RCV Id: RCV000119826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg261Gly
CA269921
NM_000277.3:c.781C>G