Canonical Allele Identifier: PA2828323106
Gene: DCX HGNC NCBI

Linked Data

ClinVar Variation Id: 158440
ClinVar RCV Id: RCV000145821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356302.1:p.Ser73Phe
CA171887
NM_001369373.1:c.218C>T