Canonical Allele Identifier: PA2828787605
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 56304
ClinVar RCV Id: RCV000049716 RCV000201581 RCV001007916 RCV001539860 RCV002514252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Thr1065Met
CA144225
NM_001378617.1:c.3194C>T