Canonical Allele Identifier: PA916037410
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Thr81Pro
CA229497
NM_001354304.2:c.241A>C