Allele Registry

Canonical Allele Identifier: PA126436

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017808

RCV000244462

RCV000285950

RCV001723573

ClinVar Variation:

16384

HGVS (amino-acid)	Matching Registered Transcripts
NP_005132.2:p.Arg478Lys	CA126434 NM_005141.5:c.1433G>A