Canonical Allele Identifier: PA229860
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102902
ClinVar RCV Id: RCV000089166 RCV000669990
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala313Thr
CA229859
NM_000277.3:c.937G>A