Allele Registry

Canonical Allele Identifier: PA126400

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017786

RCV001797589

RCV003398534

ClinVar Variation:

16366

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Met336Thr	CA126399 NM_000509.5:c.1007T>C