Canonical Allele Identifier: PA2828786697
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 501112
ClinVar RCV Id: RCV000596285 RCV002476325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Glu557Val
CA2863776
NM_001378617.1:c.1670A>T