Canonical Allele Identifier: PA2829454084
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 3160987
ClinVar RCV Id: RCV004455873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Arg290Cys
CA4348699
NM_003919.3:c.868C>T