Canonical Allele Identifier: PA915961840
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000546.2:p.Arg267Leu
CA171998
NM_000555.3:c.800G>T