Canonical Allele Identifier: PA916037527
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr204Cys
CA229653
NM_001354304.2:c.611A>G