Canonical Allele Identifier: PA2828066873
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2014569
ClinVar RCV Id: RCV002861562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349738.1:p.Gly250Arg
CA368231226
NM_001362809.2:c.748G>C
CA368231227
NM_001362809.2:c.748G>A