Canonical Allele Identifier: PA229616
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102730
ClinVar RCV Id: RCV000088979 RCV001778707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr179His
CA229615
NM_000277.3:c.535T>C