Canonical Allele Identifier: PA2825137967
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2780254
ClinVar RCV Id: RCV003598234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg158Gly
CA386299607
NM_000277.3:c.472C>G