Canonical Allele Identifier: PA106622
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102862
ClinVar RCV Id: RCV000089123 RCV000665406
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr278Asn
CA229802
NM_000277.3:c.833C>A