Canonical Allele Identifier: PA2826051594
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2777621
ClinVar RCV Id: RCV003621743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Ala470Gly
CA376071471
NM_001167945.2:c.1409C>G