Canonical Allele Identifier: PA2826204929
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 82052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182482.1:p.Arg102His
CA171926
NM_001195553.1:c.305G>A