Canonical Allele Identifier: PA2826050989
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803741
ClinVar RCV Id: RCV002467411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161407.1:p.Lys31Asn
CA367426810
NM_001167935.1:c.93A>C
CA367426811
NM_001167935.1:c.93A>T