Allele Registry

Canonical Allele Identifier: PA294629

Gene: ARX HGNC NCBI

ClinVar RCV:

RCV000144762

ClinVar Variation:

156619

HGVS (amino-acid)	Matching Registered Transcripts
NP_620689.1:p.Ala381Thr	CA294628 NM_139058.3:c.1141G>A