Canonical Allele Identifier: PA2828322530
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158446
ClinVar RCV Id: RCV000145827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Leu91Pro
CA171905
NM_001369370.1:c.272T>C