Canonical Allele Identifier: PA106723
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102477
ClinVar RCV Id: RCV000088708 RCV001194126
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr343Cys
CA229282
NM_000277.3:c.1028A>G