Allele Registry

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This migration is underway but taking longer than originally estimated.

Canonical Allele Identifier: PA172048

Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158496

ClinVar RCV Id: RCV000145880 RCV000996004 RCV003144138

ClinVar Variation Id: 422444

ClinVar RCV Id: RCV000483287

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_835365.1:p.Gly223Arg	CA172046 NM_178152.3:c.667G>A CA16621176 NM_178152.3:c.667G>C