Canonical Allele Identifier: PA2828788183
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 238281
ClinVar RCV Id: RCV000229439 RCV000385807 RCV000318552 RCV000319463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Arg1438Cys
CA2864389
NM_001378617.1:c.4312C>T