Canonical Allele Identifier: PA2828322838
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 1164037
ClinVar RCV Id: RCV001788520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356300.1:p.Asp263Gly
CA414241642
NM_001369371.1:c.788A>G