Canonical Allele Identifier: PA2825536912
Gene: SGCE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092871.1:p.Glu379Lys
CA4348622
NM_001099401.2:c.1135G>A