Canonical Allele Identifier: PA916037418
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile95Phe
CA229507
NM_001354304.2:c.283A>T