Canonical Allele Identifier: PA2828323007
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158492
ClinVar RCV Id: RCV000145876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Val210Phe
CA172038
NM_001369372.1:c.628G>T