Canonical Allele Identifier: PA2830469669
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 519506
ClinVar Variation Id: 967076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963891.1:p.Val544Leu
CA5430135
NM_201597.3:c.1630G>C
CA5430136
NM_201597.3:c.1630G>T