Canonical Allele Identifier: PA106671
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 590
ClinVar RCV Id: RCV000000621 RCV000089007
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr204Cys
CA229653
NM_000277.3:c.611A>G