Canonical Allele Identifier: PA2826051649
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775749
ClinVar RCV Id: RCV002392666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Tyr516Cys
CA5430151
NM_001167945.2:c.1547A>G