Allele Registry

Canonical Allele Identifier: PA170754

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000144152

RCV001509237

ClinVar Variation:

156105

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Ser404Pro	CA170753 NM_000509.5:c.1210T>C