Canonical Allele Identifier: PA172039
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158492
ClinVar RCV Id: RCV000145876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835364.1:p.Val210Phe
CA172038
NM_178151.3:c.628G>T