Canonical Allele Identifier: PA2826051660
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1359302
ClinVar RCV Id: RCV001872221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Arg520Leu
CA5430162
NM_001167945.2:c.1559G>T