Canonical Allele Identifier: PA916037836
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg413Pro
CA229414
NM_001354304.2:c.1238G>C