Allele Registry

Canonical Allele Identifier: PA109212

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000144152

RCV001509237

ClinVar Variation:

156105

HGVS (amino-acid)	Matching Registered Transcripts
NP_068656.2:p.Ser404Pro	CA170753 NM_021870.3:c.1210T>C