Allele Registry

Canonical Allele Identifier: PA645439180

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000337420

RCV001083911

RCV003977788

ClinVar Variation:

287220

HGVS (amino-acid)	Matching Registered Transcripts
NP_003910.1:p.Leu146Met	CA4348802 NM_003919.3:c.436T>A