Canonical Allele Identifier: PA916037785
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu365del
CA229337
NM_001354304.2:c.1092_1094del