Canonical Allele Identifier: PA916037414
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro89Ser
CA229501
NM_001354304.2:c.265C>T