Canonical Allele Identifier: PA2827282599
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447829
ClinVar RCV Id: RCV003176651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316989.1:p.Gly451Arg
CA376071554
NM_001330060.2:c.1351G>A
CA376071556
NM_001330060.2:c.1351G>C