Canonical Allele Identifier: PA171153
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 157754
ClinVar RCV Id: RCV000145053 RCV000228763 RCV002453466
ClinVar Variation Id: 2201958
ClinVar RCV Id: RCV002629855
ClinVar Variation Id: 2930060
ClinVar RCV Id: RCV003787418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620689.1:p.Ala114_Ala115del
CA171152
NM_139058.3:c.330_335del
CA874147897
NM_139058.3:c.336_341del