Canonical Allele Identifier: PA2828322900
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 11597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Asp62Asn
CA121589
NM_001369372.1:c.184G>A