Allele Registry

Canonical Allele Identifier: PA645439191

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000347102

RCV003168564

ClinVar Variation:

360992

HGVS (amino-acid)	Matching Registered Transcripts
NP_003910.1:p.Ala186Thr	CA4348768 NM_003919.3:c.556G>A