Canonical Allele Identifier: PA229284
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102478
ClinVar RCV Id: RCV000088709
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr343Phe
CA229283
NM_000277.3:c.1028A>T