Canonical Allele Identifier: PA105437
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102771
ClinVar RCV Id: RCV000089021 RCV001789759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys217Gly
CA229673
NM_000277.3:c.649T>G