Canonical Allele Identifier: PA2825137918
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1453858
ClinVar RCV Id: RCV001941587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly103Asp
CA16020764
NM_000277.3:c.308G>A