Canonical Allele Identifier: PA229629
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102738
ClinVar RCV Id: RCV000088987 RCV000674846
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly188Asp
CA229628
NM_000277.3:c.563G>A