Canonical Allele Identifier: PA645469620
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 422142
ClinVar RCV Id: RCV000484037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835366.1:p.Ile107Thr
CA16621180
NM_178153.3:c.320T>C