Canonical Allele Identifier: PA916037786
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro366His
CA229341
NM_001354304.2:c.1097C>A