Canonical Allele Identifier: PA2830467579
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963887.2:p.Gly510Ser
CA301862
NM_201593.3:c.1528G>A