Canonical Allele Identifier: PA2828066969
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 648594
ClinVar RCV Id: RCV000803351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349738.1:p.Asn355Ser
CA368228891
NM_001362809.2:c.1064A>G