Allele Registry

Canonical Allele Identifier: PA2826864777

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000639695

RCV000713250

ClinVar Variation:

420156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288068.1:p.Leu143Pro	CA16618579 NM_001301139.2:c.428T>C