Canonical Allele Identifier: PA2826051615
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 264509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Ser491Trp
CA5430123
NM_001167945.2:c.1472C>G