Canonical Allele Identifier: PA229710
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly239Ala
CA229709
NM_000277.3:c.716G>C