Canonical Allele Identifier: PA2828322500
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 932639
ClinVar RCV Id: RCV001200546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Arg56Leu
CA414246964
NM_001369370.1:c.167G>T