Canonical Allele Identifier: PA916037415
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Thr92Ile
CA229504
NM_001354304.2:c.275C>T