Canonical Allele Identifier: PA229735
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102817
ClinVar RCV Id: RCV000089072 RCV000758103
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly247Asp
CA229734
NM_000277.3:c.740G>A