Canonical Allele Identifier: PA229392
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg400Thr
CA229391
NM_000277.3:c.1199G>C