Canonical Allele Identifier: PA2828066538
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2014569
ClinVar RCV Id: RCV002861562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349737.1:p.Gly200Arg
CA368231226
NM_001362808.2:c.598G>C
CA368231227
NM_001362808.2:c.598G>A