Canonical Allele Identifier: PA916037386
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Thr63Pro
CA229473
NM_001354304.2:c.187A>C