Canonical Allele Identifier: PA2826050987
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305788
ClinVar RCV Id: RCV002874755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161407.1:p.Val20Ile
CA367426653
NM_001167935.1:c.58G>A