Canonical Allele Identifier: PA171940
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835365.1:p.Gly122Arg
CA171938
NM_178152.3:c.364G>A
CA414246550
NM_178152.3:c.364G>C