Canonical Allele Identifier: PA150863
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 126234
ClinVar RCV Id: RCV000114170 RCV000176277 RCV000515156 RCV001146036 RCV001146035 RCV000636974 RCV004529912 RCV001719852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Arg935Gln
CA150861
NM_001080522.2:c.2804G>A