Allele Registry

Canonical Allele Identifier: PA109478

Gene: DCX HGNC NCBI

ClinVar RCV:

RCV000012362

RCV000012363

ClinVar Variation:

11601

HGVS (amino-acid)	Matching Registered Transcripts
NP_000546.2:p.Arg140Leu	CA121596 NM_000555.3:c.419G>T