Canonical Allele Identifier: PA645505350
Gene: DCC HGNC NCBI

Linked Data

ClinVar Variation Id: 375284
ClinVar RCV Id: RCV000416340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005206.2:p.Arg597Pro
CA16044032
NM_005215.4:c.1790G>C