Canonical Allele Identifier: PA645487271
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Arg563Pro
CA5430130
NM_201596.3:c.1688G>C