Canonical Allele Identifier: PA2828322517
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158440
ClinVar RCV Id: RCV000145821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Ser73Phe
CA171887
NM_001369370.1:c.218C>T