Canonical Allele Identifier: PA916037379
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp59Val
CA16020736
NM_001354304.2:c.176A>T