Canonical Allele Identifier: PA2826204904
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182482.1:p.Arg76Cys
CA171890
NM_001195553.1:c.226C>T