Canonical Allele Identifier: PA2828323309
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 1709795
ClinVar RCV Id: RCV002290137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356303.1:p.Gly100Arg
CA414246693
NM_001369374.1:c.298G>C
CA414246694
NM_001369374.1:c.298G>A