Canonical Allele Identifier: PA2828786626
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_001365546.1:p.Thr515Met
CA2863732
NM_001378617.1:c.1544C>T