Canonical Allele Identifier: PA106992
Gene: CACNG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30282
ClinVar RCV Id: RCV000023217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006069.1:p.Val143Leu
CA411379456
NM_006078.5:c.427G>T
CA411379461
NM_006078.5:c.427G>C