Canonical Allele Identifier: PA2828086627
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3139758
ClinVar RCV Id: RCV004430582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350388.1:p.Pro44Ala
CA367429830
NM_001363459.2:c.130C>G