Allele Registry

Canonical Allele Identifier: PA2827383256

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000639695

RCV000713250

ClinVar Variation:

420156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333648.1:p.Leu155Pro	CA16618579 NM_001346719.1:c.464T>C