Allele Registry

Canonical Allele Identifier: PA2826051495

Gene: CACNB2 HGNC NCBI

ClinVar RCV:

RCV000170867

RCV002453580

ClinVar Variation:

190725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001161417.1:p.Phe371Leu	CA301842 NM_001167945.2:c.1113C>A CA376069990 NM_001167945.2:c.1111T>C CA376070006 NM_001167945.2:c.1113C>G