Canonical Allele Identifier: PA2829454219
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 648594
ClinVar RCV Id: RCV000803351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Asn405Ser
CA368228891
NM_003919.3:c.1214A>G