Canonical Allele Identifier: PA916037795
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 660581
ClinVar RCV Id: RCV000817803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gln375Glu
CA6748741
NM_001354304.2:c.1123C>G