Allele Registry

Canonical Allele Identifier: PA126415

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017796

ClinVar Variation:

16374

HGVS (amino-acid)	Matching Registered Transcripts
NP_068656.2:p.Asp390His	CA126413 NM_021870.3:c.1168G>C