Canonical Allele Identifier: PA229858
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102901
ClinVar RCV Id: RCV000089165 RCV001269049
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly312Asp
CA229857
NM_000277.3:c.935G>A