Allele Registry

Canonical Allele Identifier: PA145913

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV000078413

RCV000547914

RCV001288755

RCV002514376

ClinVar Variation:

92662

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Ser31Ile	CA145911 NM_000232.5:c.92G>T