Canonical Allele Identifier: PA916037662
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu280Gly
CA229808
NM_001354304.2:c.839A>G