Canonical Allele Identifier: PA208882
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 210608
ClinVar RCV Id: RCV000194608 RCV000862063 RCV001149616 RCV001149617 RCV001705077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Val660Ile
CA208880
NM_001080522.2:c.1978G>A