Canonical Allele Identifier: PA645475661
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 287246
ClinVar RCV Id: RCV000402581 RCV001202071 RCV001334751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Arg828Gln
CA2863930
NM_001080522.2:c.2483G>A