Canonical Allele Identifier: PA916037854
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala434Asp
CA229427
NM_001354304.2:c.1301C>A