Canonical Allele Identifier: PA645475631
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 291191
ClinVar RCV Id: RCV000335348 RCV001149502 RCV001248140 RCV001149503 RCV002487294 RCV002518166 RCV004537623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Thr564Met
CA2863732
NM_001080522.2:c.1691C>T