Allele Registry

Canonical Allele Identifier: PA126414

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017796

ClinVar Variation:

16374

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Asp390His	CA126413 NM_000509.5:c.1168G>C