Canonical Allele Identifier: PA172073
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158506
ClinVar RCV Id: RCV000145890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835364.1:p.Arg258Pro
CA172072
NM_178151.3:c.773G>C