Canonical Allele Identifier: PA658812542
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 537370
ClinVar RCV Id: RCV000646203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963890.2:p.Arg542Cys
CA376071535
NM_201596.3:c.1624C>T