Canonical Allele Identifier: PA109803
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 800524
ClinVar RCV Id: RCV000984506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Thr303Ile
CA414245878
NM_000555.3:c.908C>T