Canonical Allele Identifier: PA1139754959
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 971535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Val579Gly
CA5430148
NM_201596.3:c.1736T>G