Canonical Allele Identifier: PA171889
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_835365.1:p.Ser73Phe
CA171887
NM_178152.3:c.218C>T