Canonical Allele Identifier: PA2827282639
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368112
ClinVar RCV Id: RCV001874334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316989.1:p.Asp480Ala
CA5430143
NM_001330060.2:c.1439A>C