Canonical Allele Identifier: PA229792
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102854
ClinVar RCV Id: RCV000089115 RCV000672381
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro275Arg
CA229791
NM_000277.3:c.824C>G