Canonical Allele Identifier: PA2826051639
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368112
ClinVar RCV Id: RCV001874334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Asp507Ala
CA5430143
NM_001167945.2:c.1520A>C