Canonical Allele Identifier: PA2830464011
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066514
ClinVar RCV Id: RCV002934057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963864.1:p.Glu505Asp
CA5430121
NM_201570.2:c.1515G>C
CA376071650
NM_201570.2:c.1515G>T