Canonical Allele Identifier: PA916037571
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly239Ala
CA229709
NM_001354304.2:c.716G>C