Canonical Allele Identifier: PA2826204918
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 522790
ClinVar RCV Id: RCV000625954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182482.1:p.Asn96Lys
CA414246713
NM_001195553.1:c.288C>G
CA414246714
NM_001195553.1:c.288C>A