Canonical Allele Identifier: PA2580560903
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773069
ClinVar RCV Id: RCV002394725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Asn540Ser
CA376071514
NM_201596.3:c.1619A>G