Canonical Allele Identifier: PA172009
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158481
ClinVar RCV Id: RCV000145863 RCV000498232
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835365.1:p.Pro191Arg
CA172007
NM_178152.3:c.572C>G