Canonical Allele Identifier: PA2826051611
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2562816
ClinVar RCV Id: RCV003296809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Thr488Ile
CA5430122
NM_001167945.2:c.1463C>T