Allele Registry

Canonical Allele Identifier: PA126403

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017788

ClinVar Variation:

16368

HGVS (amino-acid)	Matching Registered Transcripts
NP_000500.2:p.Gln355Arg	CA126402 NM_000509.5:c.1064A>G