Canonical Allele Identifier: PA2828322628
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 427044
ClinVar RCV Id: RCV000489609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Ala251Asp
CA414241722
NM_001369370.1:c.752C>A