Canonical Allele Identifier: PA229764
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102836
ClinVar RCV Id: RCV000089095 RCV000810805
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys265Tyr
CA229763
NM_000277.3:c.794G>A