Canonical Allele Identifier: PA229502
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102641
ClinVar RCV Id: RCV000088886 RCV001857430
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro89Ser
CA229501
NM_000277.3:c.265C>T