Canonical Allele Identifier: PA916037647
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro275Ser
CA229789
NM_001354304.2:c.823C>T