Canonical Allele Identifier: PA2830465642
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773069
ClinVar RCV Id: RCV002394725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963866.2:p.Asn488Ser
CA376071514
NM_201572.4:c.1463A>G