Canonical Allele Identifier: PA2830464839
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773621
ClinVar RCV Id: RCV002397195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963865.2:p.Leu521Phe
CA376071600
NM_201571.4:c.1561C>T