Canonical Allele Identifier: PA2828322519
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 619981
ClinVar RCV Id: RCV000760181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Arg76Gly
CA414246842
NM_001369370.1:c.226C>G