Canonical Allele Identifier: PA229365
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 188933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe39del
CA229364
NM_000277.3:c.116_118del