Canonical Allele Identifier: PA2827282618
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060931
ClinVar RCV Id: RCV001370430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316989.1:p.Glu468Gly
CA376071735
NM_001330060.2:c.1403A>G