Canonical Allele Identifier: PA301863
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000715.2:p.Gly493Ser
CA301862
NM_000724.3:c.1477G>A