Canonical Allele Identifier: PA2828787660
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217598
ClinVar RCV Id: RCV000201640 RCV003330577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Val1102Ala
CA279438
NM_001378617.1:c.3305T>C