Canonical Allele Identifier: PA229512
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102648
ClinVar RCV Id: RCV000088894 RCV001580454
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile102Thr
CA229511
NM_000277.3:c.305T>C