Canonical Allele Identifier: PA229498
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102637
ClinVar RCV Id: RCV000088881 RCV001192889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr81Pro
CA229497
NM_000277.3:c.241A>C