Allele Registry

Canonical Allele Identifier: PA2741813379

Gene: SGCB HGNC NCBI

ClinVar RCV:

RCV003621191

ClinVar Variation:

2843913

HGVS (amino-acid)	Matching Registered Transcripts
NP_000223.1:p.Glu230Asp	CA356876003 NM_000232.5:c.690A>T CA356876006 NM_000232.5:c.690A>C