Canonical Allele Identifier: PA2825536830
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2731847
ClinVar RCV Id: RCV003506461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092871.1:p.Arg290Gly
CA4348701
NM_001099401.2:c.868C>G