Canonical Allele Identifier: PA2828322877
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 2579409
ClinVar RCV Id: RCV003327844

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Arg22Trp
CA414247197
NM_001369372.1:c.64C>T