Canonical Allele Identifier: PA2828323199
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158491
ClinVar RCV Id: RCV000145875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356302.1:p.His205Leu
CA172035
NM_001369373.1:c.614A>T