Canonical Allele Identifier: PA229733
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly247Arg
CA229732
NM_000277.3:c.739G>C