Allele Registry

Canonical Allele Identifier: PA2828918948

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017808

RCV000244462

RCV000285950

RCV001723573

ClinVar Variation:

16384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369691.1:p.Arg378Lys	CA126434 NM_001382762.1:c.1133G>A