Canonical Allele Identifier: PA916037835
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg413Ser
CA229411
NM_001354304.2:c.1237C>A