Canonical Allele Identifier: PA229787
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102851
ClinVar RCV Id: RCV000089112 RCV000148723
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Lys274Glu
CA229786
NM_000277.3:c.820A>G