Allele Registry

Canonical Allele Identifier: PA2826144190

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017821

ClinVar Variation:

16395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171670.1:p.Leu143Gln	CA126450 NM_001184741.1:c.428T>A