Canonical Allele Identifier: PA2830465663
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242262
ClinVar RCV Id: RCV000228679
ClinVar Variation Id: 642210
ClinVar RCV Id: RCV000795627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963866.2:p.Phe503Leu
CA10582712
NM_201572.4:c.1509T>G
CA376071662
NM_201572.4:c.1507T>C
CA376071670
NM_201572.4:c.1509T>A