Canonical Allele Identifier: PA213239
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 157765
ClinVar RCV Id: RCV000145065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620689.1:p.Arg332Leu
CA213238
NM_139058.3:c.995G>T