Allele Registry

Canonical Allele Identifier: PA2573074967

Gene: SGCG HGNC NCBI

ClinVar Variation Id: 284771

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365173.1:p.Glu198Val	CA6909734 NM_001378244.1:c.593A>T