Allele Registry

Canonical Allele Identifier: PA126409

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017790

ClinVar Variation:

16370

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Asp356Val	CA126408 NM_000509.5:c.1067A>T