Canonical Allele Identifier: PA2828322999
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 3065074
ClinVar RCV Id: RCV003990151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Lys202Glu
CA414246012
NM_001369372.1:c.604A>G