Canonical Allele Identifier: PA916037663
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu280Lys
CA251525
NM_001354304.2:c.838G>A