Canonical Allele Identifier: PA2825536524
Gene: SGCE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092870.1:p.Glu370Lys
CA4348622
NM_001099400.2:c.1108G>A