Canonical Allele Identifier: PA2830373962
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 1805112
ClinVar RCV Id: RCV002471530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835365.1:p.Val101Gly
CA414246686
NM_178152.3:c.302T>G