Canonical Allele Identifier: PA229661
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102762
ClinVar RCV Id: RCV000089012 RCV000666489
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr206Cys
CA229660
NM_000277.3:c.617A>G