Canonical Allele Identifier: PA916037599
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg252Gly
CA229742
NM_001354304.2:c.754C>G