Canonical Allele Identifier: PA229777
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102843
ClinVar RCV Id: RCV000089102 RCV000763291
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile269Asn
CA229776
NM_000277.3:c.806T>A