Allele Registry

Canonical Allele Identifier: PA2827382885

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000337420

RCV001083911

RCV003977788

ClinVar Variation:

287220

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333646.1:p.Leu146Met	CA4348802 NM_001346717.1:c.436T>A