Canonical Allele Identifier: PA2828322588
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 1473135
ClinVar RCV Id: RCV001977397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356299.1:p.Gly188Arg
CA414246093
NM_001369370.1:c.562G>A
CA414246094
NM_001369370.1:c.562G>C