Canonical Allele Identifier: PA2825138014
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1480414
ClinVar RCV Id: RCV002022060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro211Gln
CA386296671
NM_000277.3:c.632C>A