Canonical Allele Identifier: PA916075361
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 619981
ClinVar RCV Id: RCV000760181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835366.1:p.Arg76Gly
CA414246842
NM_178153.3:c.226C>G