Canonical Allele Identifier: PA229896
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102926
ClinVar RCV Id: RCV000089193 RCV002515785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe331Cys
CA229895
NM_000277.3:c.992T>G