Canonical Allele Identifier: PA2830467598
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1986582
ClinVar RCV Id: RCV002770616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963887.2:p.Glu523Asp
CA376071740
NM_201593.3:c.1569G>C
CA376071741
NM_201593.3:c.1569G>T