Canonical Allele Identifier: PA2828806724
Gene: CACNG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30282
ClinVar RCV Id: RCV000023217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365980.1:p.Val120Leu
CA411379456
NM_001379051.1:c.358G>T
CA411379461
NM_001379051.1:c.358G>C