Canonical Allele Identifier: PA645475732
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 288557
ClinVar RCV Id: RCV000263818 RCV000765761 RCV001081652 RCV004543114 RCV002521992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Ile1193Val
CA2864205
NM_001080522.2:c.3577A>G