Allele Registry

Canonical Allele Identifier: PA645439178

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000416039

RCV000689645

RCV002469145

RCV003362776

ClinVar Variation:

374642

HGVS (amino-acid)	Matching Registered Transcripts
NP_003910.1:p.Ile131Val	CA4348814 NM_003919.3:c.391A>G