Canonical Allele Identifier: PA915961783
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 422142
ClinVar RCV Id: RCV000484037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Ile188Thr
CA16621180
NM_000555.3:c.563T>C