Canonical Allele Identifier: PA2828323268
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 11603
ClinVar RCV Id: RCV000012367 RCV000012366 RCV001857334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356303.1:p.Ser47Arg
CA121600
NM_001369374.1:c.139A>C
CA414247028
NM_001369374.1:c.141T>A
CA414247029
NM_001369374.1:c.141T>G