Canonical Allele Identifier: PA2826864988
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2014569
ClinVar RCV Id: RCV002861562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288068.1:p.Gly250Arg
CA368231226
NM_001301139.2:c.748G>C
CA368231227
NM_001301139.2:c.748G>A