Canonical Allele Identifier: PA2830467658
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390567
ClinVar RCV Id: RCV001891065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963887.2:p.His547Leu
CA376072037
NM_201593.3:c.1640A>T