Canonical Allele Identifier: PA916037455
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr154His
CA229557
NM_001354304.2:c.460T>C