Canonical Allele Identifier: PA916037482
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg169His
CA286505
NM_001354304.2:c.506G>A