Canonical Allele Identifier: PA229819
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102875
ClinVar RCV Id: RCV000089136 RCV002514547
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp282Gly
CA229818
NM_000277.3:c.845A>G