Canonical Allele Identifier: PA2825137898
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2573214
ClinVar RCV Id: RCV003316903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr77His
CA386304171
NM_000277.3:c.229T>C