Allele Registry

Canonical Allele Identifier: PA2826144226

Gene: FGB HGNC NCBI

ClinVar RCV:

RCV000017815

ClinVar Variation:

16389

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171670.1:p.Leu324Arg	CA126442 NM_001184741.1:c.971T>G