Canonical Allele Identifier: PA2826051633
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 190717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161417.1:p.Val502Ile
CA301823
NM_001167945.2:c.1504G>A