Canonical Allele Identifier: PA2828786859
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 347764
ClinVar RCV Id: RCV000298157 RCV000336743 RCV000394824 RCV000731265 RCV001038299 RCV002520210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Val637Met
CA2863839
NM_001378617.1:c.1909G>A