Canonical Allele Identifier: PA2830466779
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062756
ClinVar RCV Id: RCV001372508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963884.2:p.Ser511Phe
CA376071773
NM_201590.3:c.1532C>T