Canonical Allele Identifier: PA172000
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158478
ClinVar RCV Id: RCV000145860 RCV003159105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835365.1:p.Arg186Leu
CA171998
NM_178152.3:c.557G>T