Canonical Allele Identifier: PA229577
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102698
ClinVar RCV Id: RCV000088946 RCV002251981 RCV000535090 RCV003114254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile164Val
CA229576
NM_000277.3:c.490A>G