Canonical Allele Identifier: PA2827282613
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 264509
ClinVar RCV Id: RCV000249316 RCV000479313 RCV000865251 RCV001844103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316989.1:p.Ser464Trp
CA5430123
NM_001330060.2:c.1391C>G