Canonical Allele Identifier: PA2830469613
Gene: CACNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963891.1:p.Gly524Ser
CA301862
NM_201597.3:c.1570G>A