Canonical Allele Identifier: PA916037744
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly337Val
CA229268
NM_001354304.2:c.1010G>T