Canonical Allele Identifier: PA891845375
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 585208
ClinVar RCV Id: RCV000709704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg261Leu
CA386295444
NM_000277.3:c.782G>T