Canonical Allele Identifier: PA916037714
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102902
ClinVar RCV Id: RCV000089166 RCV000669990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala313Thr
CA229859
NM_001354304.2:c.937G>A