Canonical Allele Identifier: PA2825250114
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773621
ClinVar RCV Id: RCV002397195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000715.2:p.Leu494Phe
CA376071600
NM_000724.3:c.1480C>T