Canonical Allele Identifier: PA2573206155
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1693233
ClinVar RCV Id: RCV002260492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asn223Tyr
CA16020834
NM_001354304.2:c.667A>T