Allele Registry

Canonical Allele Identifier: PA2828918939

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017816

ClinVar Variation:

16390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369691.1:p.Gly330Asp	CA126444 NM_001382762.1:c.989G>A