Canonical Allele Identifier: PA916037457
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg155His
CA229559
NM_001354304.2:c.464G>A