Allele Registry

Canonical Allele Identifier: PA2825666793

Gene: SGCD HGNC NCBI

ClinVar RCV:

RCV000808519

RCV001785727

RCV002487741

RCV003233856

ClinVar Variation:

652862

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121681.1:p.Arg30Trp	CA3530486 NM_001128209.2:c.88C>T