Canonical Allele Identifier: PA106732
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102534
ClinVar RCV Id: RCV000088767 RCV002259584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr377Cys
CA229357
NM_000277.3:c.1130A>G