Allele Registry

Canonical Allele Identifier: PA100147

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017821

ClinVar Variation:

16395

HGVS (amino-acid)	Matching Registered Transcripts
NP_005132.2:p.Leu202Gln	CA126450 NM_005141.5:c.605T>A