Canonical Allele Identifier: PA2741867098
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2643247
ClinVar RCV Id: RCV003391964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala140Glu
CA6748959
NM_001354304.2:c.419C>A