Canonical Allele Identifier: PA916037687
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92750
ClinVar RCV Id: RCV000078535 RCV000150085 RCV000588535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg297His
CA220590
NM_001354304.2:c.890G>A