Canonical Allele Identifier: PA916037809
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu390Gly
CA114367
NM_001354304.2:c.1169A>G