Canonical Allele Identifier: PA106026
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102819
ClinVar RCV Id: RCV000089074 RCV002259593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu248Pro
CA229737
NM_000277.3:c.743T>C