Canonical Allele Identifier: PA104902
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102897
ClinVar RCV Id: RCV000668228 RCV000089160
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala309Asp
CA229853
NM_000277.3:c.926C>A