Canonical Allele Identifier: PA916037653
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Met276Arg
CA229797
NM_001354304.2:c.827T>G