Canonical Allele Identifier: PA645487267
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_963890.2:p.Phe555Leu
CA10582712
NM_201596.3:c.1665T>G
CA376071662
NM_201596.3:c.1663T>C
CA376071670
NM_201596.3:c.1665T>A