Canonical Allele Identifier: PA105327
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102666
ClinVar RCV Id: RCV000088914 RCV001209954
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp143Gly
CA229538
NM_000277.3:c.428A>G