Allele Registry

Canonical Allele Identifier: PA2827382920

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000347102

RCV003168564

ClinVar Variation:

360992

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333646.1:p.Ala186Thr	CA4348768 NM_001346717.1:c.556G>A