Canonical Allele Identifier: PA2828322539
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 1805112
ClinVar RCV Id: RCV002471530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Val101Gly
CA414246686
NM_001369370.1:c.302T>G