Canonical Allele Identifier: PA916037392
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile65Val
CA229478
NM_001354304.2:c.193A>G