Canonical Allele Identifier: PA229823
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102878
ClinVar RCV Id: RCV000089139 RCV001543638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys284Arg
CA229822
NM_000277.3:c.850T>C