Allele Registry

Canonical Allele Identifier: PA2826050884

Gene: CCM2 HGNC NCBI

ClinVar RCV:

RCV000002805

ClinVar Variation:

2686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001161406.1:p.Leu140Arg	CA252400 NM_001167934.2:c.419T>G