Canonical Allele Identifier: PA2827282595
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773069
ClinVar RCV Id: RCV002394725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316989.1:p.Asn447Ser
CA376071514
NM_001330060.2:c.1340A>G