Canonical Allele Identifier: PA229399
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102567
ClinVar RCV Id: RCV000088801 RCV000758128
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile406Thr
CA229398
NM_000277.3:c.1217T>C