Canonical Allele Identifier: PA916037547
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp222Val
CA229681
NM_001354304.2:c.665A>T