Allele Registry

Canonical Allele Identifier: PA915966371

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV000805140

ClinVar Variation:

650059

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Phe233Ser	CA356875860 NM_000232.5:c.698T>C