Canonical Allele Identifier: PA658802536
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 502359
ClinVar RCV Id: RCV000593757 RCV001146865 RCV001146866 RCV001474086 RCV001755983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Cys1413Tyr
CA2864358
NM_001080522.2:c.4238G>A