Canonical Allele Identifier: PA2830373759
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 11597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835364.1:p.Asp62Asn
CA121589
NM_178151.3:c.184G>A