Canonical Allele Identifier: PA2741826194
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626151
ClinVar RCV Id: RCV003382131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025006.1:p.Thr65Ser
CA4246874
NM_001029835.2:c.193A>T
CA367427142
NM_001029835.2:c.194C>G