Canonical Allele Identifier: PA2825137934
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2682033
ClinVar RCV Id: RCV003477325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile125Thr
CA386302236
NM_000277.3:c.374T>C