Canonical Allele Identifier: PA2828786766
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 497958
ClinVar RCV Id: RCV000594861 RCV000694442 RCV000765756 RCV001148070 RCV001148071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Thr600Met
CA2863798
NM_001378617.1:c.1799C>T