Allele Registry

Canonical Allele Identifier: PA2828918658

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017821

ClinVar Variation:

16395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369688.1:p.Leu158Gln	CA126450 NM_001382759.1:c.473T>A