Canonical Allele Identifier: PA2825138236
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 987756
ClinVar RCV Id: RCV001269046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe402Val
CA16020969
NM_000277.3:c.1204T>G