Canonical Allele Identifier: PA301868
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 190730
ClinVar RCV Id: RCV000245105 RCV000458519 RCV000852602 RCV001706106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000715.2:p.Ser502Leu
CA301867
NM_000724.3:c.1505C>T