Canonical Allele Identifier: PA658679799
Gene: CACNB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 446971
ClinVar RCV Id: RCV000518041 RCV001036427 RCV001131842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000717.2:p.Ala12Ser
CA57713818
NM_000726.3:c.34G>T