Canonical Allele Identifier: PA2826051596
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 537370
ClinVar RCV Id: RCV000646203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Arg476Cys
CA376071535
NM_001167945.2:c.1426C>T