Allele Registry

Canonical Allele Identifier: PA2825536568

Gene: SGCE HGNC NCBI

ClinVar RCV:

RCV000413165

RCV003505108

ClinVar Variation:

373239

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092870.1:p.Pro440Ser	CA4348533 NM_001099400.2:c.1318C>T