Canonical Allele Identifier: PA2828086637
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2742291
ClinVar RCV Id: RCV003497596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350388.1:p.Ile105Val
CA367430229
NM_001363459.2:c.313A>G