Canonical Allele Identifier: PA2828066280
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2014569
ClinVar RCV Id: RCV002861562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349736.1:p.Gly262Arg
CA368231226
NM_001362807.2:c.784G>C
CA368231227
NM_001362807.2:c.784G>A