Allele Registry

Canonical Allele Identifier: PA126439

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017809

ClinVar Variation:

16385

HGVS (amino-acid)	Matching Registered Transcripts
NP_005132.2:p.Gly45Cys	CA126437 NM_005141.5:c.133G>T