Canonical Allele Identifier: PA916037432
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120273
ClinVar RCV Id: RCV000106354
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Thr117Ile
CA267651
NM_001354304.2:c.350C>T