Allele Registry

Canonical Allele Identifier: PA2828919053

Gene: FGB HGNC NCBI

ClinVar Allele:

31421

ClinVar RCV:

RCV000017804

RCV000852015

RCV002284174

RCV002287338

ClinVar Variation:

16382

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369693.1:p.Arg44Cys	CA126428 NM_001382764.1:c.130C>T