Allele Registry

Canonical Allele Identifier: PA2827383478

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000413165

RCV003505108

ClinVar Variation:

373239

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333648.1:p.Pro408Leu	CA4348533 NM_001346719.1:c.1223C>T