Canonical Allele Identifier: PA2825196312
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 522790
ClinVar RCV Id: RCV000625954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Asn177Lys
CA414246713
NM_000555.3:c.531C>G
CA414246714
NM_000555.3:c.531C>A