Canonical Allele Identifier: PA2828322750
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 11599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356300.1:p.Tyr125His
CA121594
NM_001369371.1:c.373T>C