Allele Registry

Canonical Allele Identifier: PA121608

Gene: DCX HGNC NCBI

ClinVar Allele:

26648

ClinVar RCV:

RCV000012373

RCV000012374

RCV000145869

RCV001552573

RCV002274878

RCV002512983

ClinVar Variation:

11609

HGVS (amino-acid)	Matching Registered Transcripts
NP_835365.1:p.Arg196His	CA121606 NM_178152.3:c.587G>A