Canonical Allele Identifier: PA916037820
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg400Lys
CA229389
NM_001354304.2:c.1199G>A