Canonical Allele Identifier: PA2828786900
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 290432
ClinVar RCV Id: RCV001087966 RCV000726483 RCV001145226 RCV001145225 RCV004537612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Arg657Gln
CA2863850
NM_001378617.1:c.1970G>A