Allele Registry

Canonical Allele Identifier: PA2828918707

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017808

RCV000244462

RCV000285950

RCV001723573

ClinVar Variation:

16384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369688.1:p.Arg434Lys	CA126434 NM_001382759.1:c.1301G>A