Canonical Allele Identifier: PA279484
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217603
ClinVar RCV Id: RCV000201684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Thr1581Ala
CA279482
NM_001080522.2:c.4741A>G