Canonical Allele Identifier: PA2580560921
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066514
ClinVar RCV Id: RCV002934057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Glu553Asp
CA5430121
NM_201596.3:c.1659G>C
CA376071650
NM_201596.3:c.1659G>T