Canonical Allele Identifier: PA2828323414
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_001356303.1:p.Asp262Gly
CA224225
NM_001369374.1:c.785A>G