Canonical Allele Identifier: PA2828323391
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_001356303.1:p.Gly223Arg
CA172046
NM_001369374.1:c.667G>A
CA16621176
NM_001369374.1:c.667G>C