Canonical Allele Identifier: PA2741867096
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2682033
ClinVar RCV Id: RCV003477325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile125Thr
CA386302236
NM_001354304.2:c.374T>C