Allele Registry

Canonical Allele Identifier: PA2828918698

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017816

ClinVar Variation:

16390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369688.1:p.Gly386Asp	CA126444 NM_001382759.1:c.1157G>A