Canonical Allele Identifier: PA915961764
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158450
ClinVar RCV Id: RCV000145831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Met82Thr
CA171917
NM_000555.3:c.245T>C