Canonical Allele Identifier: PA2826051612
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242262
ClinVar RCV Id: RCV000228679
ClinVar Variation Id: 642210
ClinVar RCV Id: RCV000795627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Phe489Leu
CA10582712
NM_001167945.2:c.1467T>G
CA376071662
NM_001167945.2:c.1465T>C
CA376071670
NM_001167945.2:c.1467T>A