Canonical Allele Identifier: PA2828788086
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 502359
ClinVar RCV Id: RCV000593757 RCV001146865 RCV001146866 RCV001474086 RCV001755983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Cys1364Tyr
CA2864358
NM_001378617.1:c.4091G>A