Canonical Allele Identifier: PA2829454183
Gene: SGCE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Asn377His
CA4348623
NM_003919.3:c.1129A>C