Canonical Allele Identifier: PA2580122503
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 1805112
ClinVar RCV Id: RCV002471530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Val182Gly
CA414246686
NM_000555.3:c.545T>G