Allele Registry

Canonical Allele Identifier: PA916043488

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000337420

RCV001083911

RCV003977788

ClinVar Variation:

287220

HGVS (amino-acid)	Matching Registered Transcripts
NP_001349737.1:p.Leu55Met	CA4348802 NM_001362808.2:c.163T>A