Canonical Allele Identifier: PA2828322922
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158445
ClinVar RCV Id: RCV000145826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Arg89Pro
CA171902
NM_001369372.1:c.266G>C