Canonical Allele Identifier: PA252399
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2684
ClinVar RCV Id: RCV000002803 RCV000517211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113631.1:p.Met1Val