Canonical Allele Identifier: PA2827383084
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1719265
ClinVar RCV Id: RCV002302025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333646.1:p.Glu370Lys
CA4348622
NM_001346717.1:c.1108G>A