Canonical Allele Identifier: PA2825138060
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 932252
ClinVar RCV Id: RCV001199976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg252Pro
CA16020854
NM_000277.3:c.755G>C