Canonical Allele Identifier: PA106059
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102826
ClinVar RCV Id: RCV000089082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu255Val
CA229746
NM_000277.3:c.763T>G