Allele Registry

Canonical Allele Identifier: PA2826864701

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000337420

RCV001083911

RCV003977788

ClinVar Variation:

287220

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288068.1:p.Leu105Met	CA4348802 NM_001301139.2:c.313T>A