Canonical Allele Identifier: PA093837
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2686
ClinVar RCV Id: RCV000002805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113631.1:p.Leu198Arg
CA252400
NM_031443.4:c.593T>G