Canonical Allele Identifier: PA105452
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102835
ClinVar RCV Id: RCV000089094 RCV002259596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys265Gly
CA229762
NM_000277.3:c.793T>G