Canonical Allele Identifier: PA2826051597
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773182
ClinVar RCV Id: RCV002396756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Arg476Gly
CA5430111
NM_001167945.2:c.1426C>G