Canonical Allele Identifier: PA2828086494
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626151
ClinVar RCV Id: RCV003382131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350387.1:p.Thr44Ser
CA4246874
NM_001363458.2:c.130A>T
CA367427142
NM_001363458.2:c.131C>G