Allele Registry

Canonical Allele Identifier: PA126492

Gene: FGA HGNC NCBI

ClinVar Allele:

31447

ClinVar RCV:

RCV000017869

RCV001753419

RCV004528118

ClinVar Variation:

16408

HGVS (amino-acid)	Matching Registered Transcripts
NP_068657.1:p.Arg573Leu	CA126489 NM_021871.4:c.1718G>T