Allele Registry

Canonical Allele Identifier: PA2826864786

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000347102

RCV003168564

ClinVar Variation:

360992

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288068.1:p.Ala145Thr	CA4348768 NM_001301139.2:c.433G>A