Canonical Allele Identifier: PA645487270
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 264509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Ser557Trp
CA5430123
NM_201596.3:c.1670C>G