Canonical Allele Identifier: PA2826204921
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158449
ClinVar RCV Id: RCV000145830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182482.1:p.Gly100Val
CA171914
NM_001195553.1:c.299G>T