Canonical Allele Identifier: PA2826051595
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773069
ClinVar RCV Id: RCV002394725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Asn474Ser
CA376071514
NM_001167945.2:c.1421A>G