Canonical Allele Identifier: PA2826051608
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066514
ClinVar RCV Id: RCV002934057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Glu487Asp
CA5430121
NM_001167945.2:c.1461G>C
CA376071650
NM_001167945.2:c.1461G>T