Canonical Allele Identifier: PA645469655
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158481
ClinVar RCV Id: RCV000145863 RCV000498232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835366.1:p.Pro191Arg
CA172007
NM_178153.3:c.572C>G