Canonical Allele Identifier: PA2825138036
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 932251
ClinVar RCV Id: RCV001199975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln226Lys
CA16020836
NM_000277.3:c.676C>A