Allele Registry

Canonical Allele Identifier: PA2828918631

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017809

ClinVar Variation:

16385

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369688.1:p.Gly45Cys	CA126437 NM_001382759.1:c.133G>T