Canonical Allele Identifier: PA916037703
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu308Phe
CA229851
NM_001354304.2:c.922C>T