Canonical Allele Identifier: PA097778
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217595
ClinVar RCV Id: RCV000201720 RCV001234448 RCV003993887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Gln1096His
CA279501
NM_001080522.2:c.3288G>C
CA356418450
NM_001080522.2:c.3288G>T