Canonical Allele Identifier: PA915983632
Gene: CACNB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 204938
ClinVar RCV Id: RCV000186842 RCV000376086 RCV000526121 RCV000321619 RCV004020261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139270.1:p.Ser3Phe
CA313402
NM_001145798.2:c.8C>T