Canonical Allele Identifier: PA269922
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 133314
ClinVar RCV Id: RCV000119826

Amino-acid Alleles

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