Canonical Allele Identifier: PA2828322913
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 619981
ClinVar RCV Id: RCV000760181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356301.1:p.Arg76Gly
CA414246842
NM_001369372.1:c.226C>G