Canonical Allele Identifier: PA2825196314
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 996565
ClinVar RCV Id: RCV001291057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Leu178Val
CA414246711
NM_000555.3:c.532C>G