Canonical Allele Identifier: PA106017
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102807
ClinVar RCV Id: RCV000089058 RCV000411222
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu242Phe
CA229718
NM_000277.3:c.724C>T