Allele Registry

Canonical Allele Identifier: PA126422

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017800

RCV000791084

RCV000851827

RCV000963143

RCV001144043

RCV002222000

ClinVar Variation:

16378

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Gly191Arg	CA126421 NM_000509.5:c.571G>A CA358536807 NM_000509.5:c.571G>C