Canonical Allele Identifier: PA658663478
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 446524
ClinVar RCV Id: RCV000515792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg169Pro
CA386299458
NM_000277.3:c.506G>C