Canonical Allele Identifier: PA916037553
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro225Thr
CA229685
NM_001354304.2:c.673C>A