Canonical Allele Identifier: PA2580223296
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2137404
ClinVar RCV Id: RCV003062533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser391Ile
CA16020957
NM_001354304.2:c.1172G>T