Canonical Allele Identifier: PA2825138091
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2137406
ClinVar RCV Id: RCV003041167 RCV003229102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu280Ala
CA16020696
NM_000277.3:c.839A>C