Canonical Allele Identifier: PA172025
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158487
ClinVar RCV Id: RCV000145871 RCV000478870
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835365.1:p.Leu199Pro
CA172023
NM_178152.3:c.596T>C