Canonical Allele Identifier: PA2828786767
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 347761
ClinVar RCV Id: RCV000270412 RCV000379021 RCV001339478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Thr600Arg
CA2863797
NM_001378617.1:c.1799C>G