Canonical Allele Identifier: PA2826204920
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 996565
ClinVar RCV Id: RCV001291057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182482.1:p.Leu97Val
CA414246711
NM_001195553.1:c.289C>G