Allele Registry

Canonical Allele Identifier: PA126401

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017786

RCV001797589

RCV003398534

ClinVar Variation:

16366

HGVS (amino-acid)	Matching Registered Transcripts
NP_068656.2:p.Met336Thr	CA126399 NM_021870.3:c.1007T>C