Canonical Allele Identifier: PA645475808
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 238282
ClinVar RCV Id: RCV000233494 RCV000765763 RCV001329603 RCV001753692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Arg1618Cys
CA2864491
NM_001080522.2:c.4852C>T