Canonical Allele Identifier: PA2828323206
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158496
ClinVar Variation Id: 422444
ClinVar RCV Id: RCV000483287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356302.1:p.Gly223Arg
CA172046
NM_001369373.1:c.667G>A
CA16621176
NM_001369373.1:c.667G>C