Canonical Allele Identifier: PA2827282668
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436599
ClinVar RCV Id: RCV001946397 RCV002397964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316989.1:p.Glu500Asp
CA203167312
NM_001330060.2:c.1500G>C
CA376072182
NM_001330060.2:c.1500G>T