Canonical Allele Identifier: PA2826051628
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062756
ClinVar RCV Id: RCV001372508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Ser499Phe
CA376071773
NM_001167945.2:c.1496C>T