Canonical Allele Identifier: PA916037346
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser16Pro
CA229564
NM_001354304.2:c.46T>C