Canonical Allele Identifier: PA915983648
Gene: CACNB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 204939
ClinVar RCV Id: RCV000186843 RCV000271279 RCV000384411 RCV000471900 RCV000515246 RCV002054189 RCV004537572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139270.1:p.Pro15Arg
CA313404
NM_001145798.2:c.44C>G