Canonical Allele Identifier: PA2830469726
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963891.1:p.Glu569Asp
CA203167312
NM_201597.3:c.1707G>C
CA376072182
NM_201597.3:c.1707G>T