Canonical Allele Identifier: PA104863
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102831
ClinVar RCV Id: RCV000089088 RCV000411173
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala259Thr
CA229755
NM_000277.3:c.775G>A