Allele Registry

Canonical Allele Identifier: PA126406

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017789

ClinVar Variation:

16369

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Asp356Tyr	CA126405 NM_000509.5:c.1066G>T