Canonical Allele Identifier: PA658663410
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 458080
ClinVar RCV Id: RCV000529284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr24Cys
CA6749047
NM_000277.3:c.71A>G