Canonical Allele Identifier: PA172027
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158488
ClinVar RCV Id: RCV000145872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835364.1:p.Thr203Ala
CA172026
NM_178151.3:c.607A>G