Canonical Allele Identifier: PA2825250121
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242262
ClinVar RCV Id: RCV000228679
ClinVar Variation Id: 642210
ClinVar RCV Id: RCV000795627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000715.2:p.Phe500Leu
CA10582712
NM_000724.3:c.1500T>G
CA376071662
NM_000724.3:c.1498T>C
CA376071670
NM_000724.3:c.1500T>A