Canonical Allele Identifier: PA916037709
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu311Pro
CA251524
NM_001354304.2:c.932T>C