Canonical Allele Identifier: PA915961924
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 96553
ClinVar RCV Id: RCV000082707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Asp343Gly
CA224225
NM_000555.3:c.1028A>G