Canonical Allele Identifier: PA645475658
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 238276
ClinVar RCV Id: RCV000726192 RCV001150183 RCV001150184 RCV001150185 RCV000765757 RCV001084783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Gly776Arg
CA2863889
NM_001080522.2:c.2326G>A
CA356417544
NM_001080522.2:c.2326G>C