Canonical Allele Identifier: PA645505383
Gene: DCC HGNC NCBI

Linked Data

ClinVar Variation Id: 375287
ClinVar RCV Id: RCV000416342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005206.2:p.Ala893Thr
CA16044036
NM_005215.4:c.2677G>A