Canonical Allele Identifier: PA2825138180
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327565
ClinVar RCV Id: RCV001789827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Lys361Gln
CA16020936
NM_000277.3:c.1081A>C