Canonical Allele Identifier: PA2826051634
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 519506
ClinVar RCV Id: RCV000617371 RCV001193384 RCV002531799
ClinVar Variation Id: 967076
ClinVar RCV Id: RCV001241897 RCV002402765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Val502Leu
CA5430135
NM_001167945.2:c.1504G>C
CA5430136
NM_001167945.2:c.1504G>T