Canonical Allele Identifier: PA2828066609
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1719265
ClinVar RCV Id: RCV002302025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349737.1:p.Glu279Lys
CA4348622
NM_001362808.2:c.835G>A