Canonical Allele Identifier: PA347155
Gene: DCC HGNC NCBI

Linked Data

ClinVar Variation Id: 187793
ClinVar RCV Id: RCV000192076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005206.2:p.Gly803Arg
CA347154
NM_005215.4:c.2407G>A
CA402471661
NM_005215.4:c.2407G>C