Allele Registry

Canonical Allele Identifier: PA916043496

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000347102

RCV003168564

ClinVar Variation:

360992

HGVS (amino-acid)	Matching Registered Transcripts
NP_001349737.1:p.Ala95Thr	CA4348768 NM_001362808.2:c.283G>A