Canonical Allele Identifier: PA2825137880
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1693243
ClinVar RCV Id: RCV002260502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu66Lys
CA16020744
NM_000277.3:c.196G>A