Allele Registry

Canonical Allele Identifier: PA126411

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017795

ClinVar Variation:

16373

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Arg401Gly	CA126410 NM_000509.5:c.1201C>G