Allele Registry

Canonical Allele Identifier: PA209569

Gene: CACNB4 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000195021

RCV000286296

RCV000341315

RCV000515346

RCV000660363

RCV000724000

RCV001079683

RCV004535183

ClinVar Variation:

193120

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000717.2:p.Ser2Phe	CA209568 NM_000726.3:c.5C>T