Allele Registry

Canonical Allele Identifier: PA109564

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_000546.2:p.Arg277His	CA121606 NM_000555.3:c.830G>A