Canonical Allele Identifier: PA916037765
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu347Phe
CA229296
NM_001354304.2:c.1039C>T