Canonical Allele Identifier: PA916037840
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp415Asn
CA114364
NM_001354304.2:c.1243G>A