Allele Registry

Canonical Allele Identifier: PA112817

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000639695

RCV000713250

ClinVar Variation:

420156

HGVS (amino-acid)	Matching Registered Transcripts
NP_003910.1:p.Leu184Pro	CA16618579 NM_003919.3:c.551T>C