Canonical Allele Identifier: PA2827327766
Gene: CACNB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 204927
ClinVar RCV Id: RCV000724955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317047.1:p.Gly126Arg
CA313382
NM_001330118.1:c.376G>A
CA348801588
NM_001330118.1:c.376G>C