Allele Registry

Canonical Allele Identifier: PA126404

Gene: FGG HGNC NCBI

ClinVar RCV:

RCV000017788

ClinVar Variation:

16368

HGVS (amino-acid)	Matching Registered Transcripts
NP_068656.2:p.Gln355Arg	CA126402 NM_021870.3:c.1064A>G