Canonical Allele Identifier: PA109440
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 11610
ClinVar RCV Id: RCV000012376 RCV000012375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Ala152Ser
CA121609
NM_000555.3:c.454G>T