Allele Registry

Canonical Allele Identifier: PA2830373750

Gene: DCX HGNC NCBI

ClinVar Variation Id: 11603

HGVS (amino-acid)	Matching Registered Transcripts
NP_835364.1:p.Ser47Arg	CA121600 NM_178151.3:c.139A>C CA414247028 NM_178151.3:c.141T>A CA414247029 NM_178151.3:c.141T>G