Canonical Allele Identifier: PA2826050882
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 562020
ClinVar RCV Id: RCV000681486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161406.1:p.Leu137Arg
CA367430423
NM_001167934.2:c.410T>G