Canonical Allele Identifier: PA916037651
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102856
ClinVar RCV Id: RCV000089117 RCV000664652
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Met276Val
CA229794
NM_001354304.2:c.826A>G