Canonical Allele Identifier: PA2828322945
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Gly122Arg
CA171938
NM_001369372.1:c.364G>A
CA414246550
NM_001369372.1:c.364G>C