Canonical Allele Identifier: PA916037574
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly239Val
CA229711
NM_001354304.2:c.716G>T