Canonical Allele Identifier: PA301869
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_963884.2:p.Ser503Leu
CA301867
NM_201590.3:c.1508C>T