Allele Registry

Canonical Allele Identifier: PA2580111048

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV002300733

ClinVar Variation:

1712561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Val232Ile	CA356875988 NM_000232.5:c.694G>A