Canonical Allele Identifier: PA915961782
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 210829
ClinVar RCV Id: RCV000193684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Tyr186dup
CA207338
NM_000555.3:c.556_558dup