Canonical Allele Identifier: PA210340
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217604
ClinVar RCV Id: RCV000201775 RCV001853233
ClinVar Variation Id: 1453471
ClinVar RCV Id: RCV002037916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Glu1000Val
CA210338
NM_001080522.2:c.2999A>T
CA2573137613
NM_001080522.2:c.2999_3000delinsTT