Canonical Allele Identifier: PA916072519
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 660461
ClinVar RCV Id: RCV000817657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620689.1:p.Asp140Tyr
CA327733056
NM_139058.3:c.418G>T