Canonical Allele Identifier: PA105213
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg408Gln
CA229404
NM_000277.3:c.1223G>A