Canonical Allele Identifier: PA2828086650
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_001350388.1:p.Leu140Arg
CA252400
NM_001363459.2:c.419T>G