Canonical Allele Identifier: PA229687
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102780
ClinVar RCV Id: RCV000089031 RCV001543660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro225Ala
CA229686
NM_000277.3:c.673C>G