Canonical Allele Identifier: PA645475647
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 347761
ClinVar RCV Id: RCV000270412 RCV000379021 RCV001339478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Thr649Arg
CA2863797
NM_001080522.2:c.1946C>G