Canonical Allele Identifier: PA2826051599
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447829
ClinVar RCV Id: RCV003176651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Gly478Arg
CA376071554
NM_001167945.2:c.1432G>A
CA376071556
NM_001167945.2:c.1432G>C