Canonical Allele Identifier: PA2826051604
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Gly482Ser
CA301862
NM_001167945.2:c.1444G>A