Canonical Allele Identifier: PA916037706
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala309Asp
CA229853
NM_001354304.2:c.926C>A