Allele Registry

Canonical Allele Identifier: PA2827382293

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000639695

RCV000713250

ClinVar Variation:

420156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333642.1:p.Leu220Pro	CA16618579 NM_001346713.1:c.659T>C