Canonical Allele Identifier: PA916037486
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.His170Asp
CA273111
NM_001354304.2:c.508C>G