Canonical Allele Identifier: PA2828322538
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158451
ClinVar RCV Id: RCV000145832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Val101Met
CA171920
NM_001369370.1:c.301G>A