Canonical Allele Identifier: PA2826205026
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 96553
ClinVar RCV Id: RCV000082707
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182482.1:p.Asp262Gly
CA224225
NM_001195553.1:c.785A>G