Canonical Allele Identifier: PA229352
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102529
ClinVar RCV Id: RCV000088762 RCV002259583
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala373Thr
CA229351
NM_000277.3:c.1117G>A