Canonical Allele Identifier: PA313398
Gene: CACNB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 204935
ClinVar RCV Id: RCV000459626 RCV000186839 RCV003233493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000717.2:p.Arg452Lys
CA313397
NM_000726.3:c.1355G>A