Canonical Allele Identifier: PA645475805
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 421347
ClinVar RCV Id: RCV000479727 RCV001053315 RCV002525868 RCV002496867 RCV004541523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Ala1577Thr
CA2864468
NM_001080522.2:c.4729G>A