Canonical Allele Identifier: PA2828788073
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217609
ClinVar RCV Id: RCV000201617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Ile1360Thr
CA279416
NM_001378617.1:c.4079T>C