Allele Registry

Canonical Allele Identifier: PA100157

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017815

ClinVar Variation:

16389

HGVS (amino-acid)	Matching Registered Transcripts
NP_005132.2:p.Leu383Arg	CA126442 NM_005141.5:c.1148T>G