Canonical Allele Identifier: PA658812548
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 519506
ClinVar Variation Id: 967076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Val568Leu
CA5430135
NM_201596.3:c.1702G>C
CA5430136
NM_201596.3:c.1702G>T