Canonical Allele Identifier: PA2826050979
Gene: CCM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2684
ClinVar RCV Id: RCV000002803 RCV000517211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161407.1:p.Met1Val