Canonical Allele Identifier: PA229827
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102880
ClinVar RCV Id: RCV000089141 RCV000758134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu286Lys
CA229826
NM_000277.3:c.856G>A