Allele Registry

Canonical Allele Identifier: PA109192

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017790

ClinVar Variation:

16370

HGVS (amino-acid)	Matching Registered Transcripts
NP_068656.2:p.Asp356Val	CA126408 NM_021870.3:c.1067A>T