Canonical Allele Identifier: PA106469
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102787
ClinVar RCV Id: RCV000089038 RCV001857431
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser231Phe
CA229695
NM_000277.3:c.692C>T