Canonical Allele Identifier: PA916037623
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Cys265Gly
CA229762
NM_001354304.2:c.793T>G