Canonical Allele Identifier: PA2826051647
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1504916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Asp514Gly
CA5430149
NM_001167945.2:c.1541A>G